Composés oxacycliques
Anhydride phtalique, 99%
CAS: 85-44-9 Formule moléculaire: C8H4O3 Poids moléculaire (g/mol): 148.12 Numéro MDL: MFCD00005918 Clé InChI: LGRFSURHDFAFJT-UHFFFAOYSA-N Synonyme: phthalic anhydride,isobenzofuran-1,3-dione,1,3-isobenzofurandione,1,3-dioxophthalan,1,3-phthalandione,phthalsaeureanhydrid,phthalic acid anhydride,o-phthalic acid anhydride,phthalandione,retarder esen PubChem CID: 6811 ChEBI: CHEBI:36605 SOURIRES: O=C1OC(=O)C2=CC=CC=C12
4-Oxo-4H-1-benzopyran-2-carboxylique, 97%
CAS: 4940-39-0 Formule moléculaire: C10H6O4 Poids moléculaire (g/mol): 190.15 Numéro MDL: MFCD00006838 Clé InChI: RVMGXWBCQGAWBR-UHFFFAOYSA-N Synonyme: chromocarb,chromone-2-carboxylic acid,4-oxo-4h-chromene-2-carboxylic acid,4-oxo-4h-1-benzopyran-2-carboxylic acid,atremon,chromonecarboxylic acid,lp-1,chromocarb inn:dcf,2-chromonecarboxylic acid,chromocarbe inn-french PubChem CID: 2741 Nom de l’IUPAC: Acide 4-oxochromène-2-carboxylique SOURIRES: C1=CC=C2C(=C1)C(=O)C=C(O2)C(=O)O
alpha-naphthoflavone, 97%
CAS: 604-59-1 Formule moléculaire: C19H12O2 Poids moléculaire (g/mol): 272.29 Numéro MDL: MFCD00004985 Clé InChI: VFMMPHCGEFXGIP-UHFFFAOYSA-N Synonyme: alpha-naphthoflavone,7,8-benzoflavone,2-phenyl-4h-benzo h chromen-4-one,alpha-naphthylflavone,2-phenylbenzo h chromen-4-one,benzo h flavone,4h-naphtho 1,2-b pyran-4-one, 2-phenyl,.alpha.-naphthoflavone,2-phenyl-benzo h chromen-4-one,2-phenyl-4h-naphtho 1,2-b pyran-4-one PubChem CID: 11790 ChEBI: CHEBI:76995 Nom de l’IUPAC: 2-phénylbenzo[h]chromène-4-one SOURIRES: C1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C4=CC=CC=C4C=C3
Acide chromone-3-carboxylique, 98%
CAS: 39079-62-4 Formule moléculaire: C10H6O4 Poids moléculaire (g/mol): 190.154 Numéro MDL: MFCD00017338 Clé InChI: PCIITXGDSHXTSN-UHFFFAOYSA-N Synonyme: chromone-3-carboxylic acid,4-oxo-4h-chromene-3-carboxylic acid,4-oxo-4h-1-benzopyran-3-carboxylic acid,maybridge1_005842,3-carboxychromone,d04tgn,acmc-1ad65,4-oxo-chromene-3-carboxylic acid,4h-chromen-4-one-3-carboxylic acid PubChem CID: 181620 Nom de l’IUPAC: Acide 4-oxochromène-3-carboxylique SOURIRES: C1=CC=C2C(=C1)C(=O)C(=CO2)C(=O)O
Bis(2-oxo-3-oxazolidinyl)chlorure phosphinique, 97%
CAS: 68641-49-6 Formule moléculaire: C6H8ClN2O5P Poids moléculaire (g/mol): 254.563 Numéro MDL: MFCD00010077 Clé InChI: KLDLRDSRCMJKGM-UHFFFAOYSA-N Synonyme: bis 2-oxo-3-oxazolidinyl phosphinic chloride,bop-cl,bis 2-oxooxazolidin-3-yl phosphinic chloride,ccris 2607,phosphinic chloride, bis 2-oxo-3-oxazolidinyl,bis 2-oxo-3-oxazolidinyl phosphonic chloride,bis 2-oxo-1,3-oxazolidin-3-yl phosphinoyl chloride,bis-2-oxo-3-oxazolidinyl phosphinic chloride,n,n-bis 2-oxo-3-oxazolidinyl phosphinic chloride,bis 2-oxo-3-oxazolidinyl phosphinic chloride bop-cl PubChem CID: 152842 Nom de l’IUPAC: 3-[chloro-(2-oxo-1,3-oxazolidin-3-yl)phosphoryl]-1,3-oxazolidine-2-one SOURIRES: C1COC(=O)N1P(=O)(N2CCOC2=O)Cl
2,2,4-Triméthyl-1,3-dioxolane, 99%
CAS: 1193-11-9 Formule moléculaire: C6H12O2 Poids moléculaire (g/mol): 116.16 Numéro MDL: MFCD00090841 Clé InChI: ALTFLAPROMVXNX-UHFFFAOYNA-N PubChem CID: 62384 Nom de l’IUPAC: 2,2,4-triméthyl-1,3-dioxolane SOURIRES: CC1COC(C)(C)O1
Acide coumalique, 97%
CAS: 500-05-0 Formule moléculaire: C6H4O4 Poids moléculaire (g/mol): 140.09 Numéro MDL: MFCD00006644 Clé InChI: ORGPJDKNYMVLFL-UHFFFAOYSA-N Synonyme: coumalic acid,2-oxo-2h-pyran-5-carboxylic acid,cumalic acid,2h-pyran-5-carboxylic acid, 2-oxo,2-oxopyran-5-carboxylic acid,unii-ob1jpy343g,2-pyrone-5-carboxylic acid,alpha-pyrone-5-carboxylic acid,.alpha.-pyrone-5-carboxylic acid,ob1jpy343g PubChem CID: 68141 SOURIRES: OC(=O)C1=COC(=O)C=C1
N-BOC-3-(4-Cyanophényl)oxaziridine, 98+%
CAS: 150884-56-3 Formule moléculaire: C13H14N2O3 Poids moléculaire (g/mol): 246.27 Numéro MDL: MFCD00800493 Clé InChI: ACXPNVRTMHEHMQ-UHFFFAOYSA-N Synonyme: n-boc-3-4-cyanophenyl oxaziridine,tert-butyl 3-4-cyanophenyl-1,2-oxaziridine-2-carboxylate,tert-butyl 3-4-cyanophenyl oxaziridine-2-carboxylate,2-oxaziridinecarboxylicacid, 3-4-cyanophenyl-, 1,1-dimethylethyl ester, 2r,3s-rel-9ci,acmc-20n62r,n-boc-3-4-cyanophenyl oxaziridine, 98+%,2-tert-butoxycarbonyl-3-4-cyanophenyl oxaziridine,n-tert-butoxycarbonyl-3-4-cyanophenyl-oxaziridine,3-4-cyano-phenyl-oxaziridine-2-carboxylic acid tert-butyl ester,3-4-cyano-phenyl oxaziridine-2-carboxylic acid tert-butyl ester PubChem CID: 2725038 Nom de l’IUPAC: Tert-butyl 3-(4-cyanophényl)oxaziridine-2-carboxylate SOURIRES: CC(C)(C)OC(=O)N1C(O1)C2=CC=C(C=C2)C#N
Phthalide, 99%
CAS: 87-41-2 Numéro MDL: MFCD00005906 Clé InChI: WNZQDUSMALZDQF-UHFFFAOYSA-N Synonyme: phthalide,isobenzofuran-1 3h-one,1 3h-isobenzofuranone,1-phthalanone,phthalolactone,2-benzofuran-1 3h-one,isobenzofuranone,phthalanone,3h-isobenzofuran-1-one,2-hydroxymethylbenzoic acid, gamma-lactone PubChem CID: 6885 ChEBI: CHEBI:38085 Nom de l’IUPAC: 3H-2-benzofuran-1-one SOURIRES: C1C2=CC=CC=C2C(=O)O1
Sulfite de glycol, 98%
CAS: 3741-38-6 Formule moléculaire: C2H4O3S Poids moléculaire (g/mol): 108.11 Numéro MDL: MFCD00005354 Clé InChI: WDXYVJKNSMILOQ-UHFFFAOYSA-N Synonyme: ethylene sulfite,glycol sulfite,1,3,2-dioxathiolane, 2-oxide,glycolsulfite,1,2-ethylene sulfite,cyclic ethylene sulfite,ethylene glycol cyclic sulfite,ethylene glycol, cyclic sulfite,ethylene sulphite,sulfurous acid, cyclic ester with ethylene glycol PubChem CID: 77342 Nom de l’IUPAC: 1,3,2-dioxathiolane 2-oxyde SOURIRES: O=S1OCCO1
Anhydride phtalique, SCA, 99,0-100,2%
CAS: 85-44-9 Formule moléculaire: C8H4O3 Poids moléculaire (g/mol): 148.12 Numéro MDL: MFCD00005918 Clé InChI: LGRFSURHDFAFJT-UHFFFAOYSA-N Synonyme: phthalic anhydride,isobenzofuran-1,3-dione,1,3-isobenzofurandione,1,3-dioxophthalan,1,3-phthalandione,phthalsaeureanhydrid,phthalic acid anhydride,o-phthalic acid anhydride,phthalandione,retarder esen PubChem CID: 6811 ChEBI: CHEBI:36605 Nom de l’IUPAC: 2-benzofurane-1,3-dione SOURIRES: O=C1OC(=O)C2=CC=CC=C12
Psoralen, 97%, Thermo Scientific Chemicals
CAS: 66-97-7 Formule moléculaire: C11H6O3 Poids moléculaire (g/mol): 186.17 Numéro MDL: MFCD00010520 Clé InChI: ZCCUUQDIBDJBTK-UHFFFAOYSA-N Synonyme: psoralen,ficusin,7h-furo 3,2-g chromen-7-one,furocoumarin,psoralene,7h-furo 3,2-g 1 benzopyran-7-one,psorline-p,6,7-furanocoumarin,furo 3,2-g chromen-7-one,furo 3,2-g coumarin PubChem CID: 6199 ChEBI: CHEBI:27616 Nom de l’IUPAC: 7H-furo[3,2-g]chromen-7-one SOURIRES: O=C1OC2=CC3=C(C=CO3)C=C2C=C1
2,3-O-Isopropylidène-D-glycéraldéhyde, 50% p/w en dichlorométhane
CAS: 15186-48-8 Formule moléculaire: C6H10O3 Poids moléculaire (g/mol): 130.143 Numéro MDL: MFCD00269682 Clé InChI: YSGPYVWACGYQDJ-YFKPBYRVSA-N Synonyme: r-+-2,2-dimethyl-1,3-dioxolane-4-carboxaldehyde,4r-2,2-dimethyl-1,3-dioxolane-4-carbaldehyde,r-2,2-dimethyl-1,3-dioxolane-4-carbaldehyde,r-+-glyceraldehyde acetonide,1,3-dioxolane-4-carboxaldehyde, 2,2-dimethyl-, r,acetone d-glyceraldehyde,+-2,2-dimethyl-1,3-dioxolane-4-carboxaldehyde,1,3-dioxolane-4-carboxaldehyde, 2,2-dimethyl-, 4r,4r-2,2-dimethyl-1,3-dioxolan-4-carbaldehyd,pubchem5767 PubChem CID: 259712 Nom de l’IUPAC: (4R)-2,2-diméthyl-1,3-dioxolane-4-carbaldehyde SOURIRES: CC1(OCC(O1)C=O)C
Acide oxazole-5-carboxylique, 98+%
CAS: 118994-90-4 Formule moléculaire: C4H3NO3 Poids moléculaire (g/mol): 113.072 Numéro MDL: MFCD04114931 Clé InChI: QCGMEWVZBGQOFN-UHFFFAOYSA-N Synonyme: oxazole-5-carboxylic acid,5-oxazolecarboxylic acid,5-oxazolecarboxylicacid,5-carboxy-1,3-oxazole,oxazole-5-carboxylicacid,5-carboxyoxazole,acmc-209a0v,ksc173g8b,1,3-oxazole-5-carboxylic acid PubChem CID: 16340557 Nom de l’IUPAC: 1,3-oxazole-5-acide carboxylique SOURIRES: C1=C(OC=N1)C(=O)O
(2-Oxo-3-benzoxazolyl)acide acétique, 97%
CAS: 13610-49-6 Formule moléculaire: C9H7NO4 Poids moléculaire (g/mol): 193.158 Numéro MDL: MFCD01547452 Clé InChI: PHIUXGVYFVAGTC-UHFFFAOYSA-N Synonyme: 2-oxo-1,3-benzoxazol-3 2h-yl acetic acid,2-oxo-benzooxazol-3-yl-acetic acid,2-2-oxobenzo d oxazol-3 2h-yl acetic acid,2 3h-benzoxazolone-3-yl acetic acid,2-oxo-1,3-benzoxazol-3-yl acetic acid,2-2-oxo-2,3-dihydro-1,3-benzoxazol-3-yl acetic acid,2-2-oxo-3-hydrobenzoxazol-3-yl acetic acid,3 2h-benzoxazoleacetic acid,2-oxo,3-benzoxazolonyl acetic acid,tos-bb-0934 PubChem CID: 737119 Nom de l’IUPAC: 2-(2-oxo-1,3-benzoxazol-3-yl)acide acétique SOURIRES: C1=CC=C2C(=C1)N(C(=O)O2)CC(=O)O