missing translation for 'onlineSavingsMsg'
Learn More
Learn More
N-Boc-propargylamine, 97%
CAS: 92136-39-5 | C8H13NO2 | 155.197 g/mol
$63.38 - $616.10
Chemical Identifiers
| CAS | 92136-39-5 |
|---|---|
| Molecular Formula | C8H13NO2 |
| Molecular Weight (g/mol) | 155.197 |
| MDL Number | MFCD07367245 |
| InChI Key | DSPYCWLYGXGJNJ-UHFFFAOYSA-N |
| Synonym | n-boc-propargylamine, n-tert-butoxycarbonyl propargylamine, n-boc-prop-2-ynylamine, tert-butyl prop-2-yn-1-ylcarbamate, n-boc-propargyl amine, tert-butyl n-prop-2-yn-1-yl carbamate, tert-butyl prop-2-ynylcarbamate, n-boc-2-propyn-1-amine, n-boc propargyl amine, prop-2-ynyl-carbamic acid tert-butyl ester |
| PubChem CID | 11073648 |
| IUPAC Name | tert-butyl N-prop-2-ynylcarbamate |
| SMILES | CC(C)(C)OC(=O)NCC#C |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|---|---|---|---|---|---|---|---|---|---|
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|
AAH5340603
|
Thermo Scientific Chemicals
H5340603 |
1 g |
Each for $63.38
|
|
|||||
|
AAH5340606
|
Thermo Scientific Chemicals
H5340606 |
5 g |
Each for $185.36
|
|
|||||
|
AAH5340614
|
Thermo Scientific Chemicals
H5340614 |
25 g |
Each for $616.10
|
|
|||||
Description
N-Boc-propargylamine is used to prepare triazolobenzylidene-thiazolopyrimidines. which act as CDC25 phosphatase inhibitors. Further, it is used for the synthesis of beta-glucan polysaccharide analogs. In addition to this, it is involved in the Pauson-Khand (PK) reaction of norbornadiene and N-Boc-propargylamine to prepare 4,5-disubstituted cyclopentenones .
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
ApplicationsN-Boc-propargylamine is used to prepare triazolobenzylidene-thiazolopyrimidines. which act as CDC25 phosphatase inhibitors. Further, it is used for the synthesis of beta-glucan polysaccharide analogs. In addition to this, it is involved in the Pauson-Khand (PK) reaction of norbornadiene and N-Boc-propargylamine to prepare 4,5-disubstituted cyclopentenones .
Solubility
Soluble in chloroform.
Notes
Moisture sensitive. Incompatible with oxidizing agents. Store in a cool place.
Chemical Identifiers
| 92136-39-5 | |
| 155.197 | |
| DSPYCWLYGXGJNJ-UHFFFAOYSA-N | |
| 11073648 | |
| CC(C)(C)OC(=O)NCC#C |
| C8H13NO2 | |
| MFCD07367245 | |
| n-boc-propargylamine, n-tert-butoxycarbonyl propargylamine, n-boc-prop-2-ynylamine, tert-butyl prop-2-yn-1-ylcarbamate, n-boc-propargyl amine, tert-butyl n-prop-2-yn-1-yl carbamate, tert-butyl prop-2-ynylcarbamate, n-boc-2-propyn-1-amine, n-boc propargyl amine, prop-2-ynyl-carbamic acid tert-butyl ester | |
| tert-butyl N-prop-2-ynylcarbamate |
Specifications
| 40°C to 44°C | |
| C8H13NO2 | |
| MFCD07367245 | |
| Soluble in chloroform. | |
| CC(C)(C)OC(=O)NCC#C | |
| 1 g | |
| 93°C (199°F) | |
| 155.2 | |
| 97% |
| 92136-39-5 | |
| HC≡CCH2NHCO2C(CH3)3 | |
| n-boc-propargylamine, n-tert-butoxycarbonyl propargylamine, n-boc-prop-2-ynylamine, tert-butyl prop-2-yn-1-ylcarbamate, n-boc-propargyl amine, tert-butyl n-prop-2-yn-1-yl carbamate, tert-butyl prop-2-ynylcarbamate, n-boc-2-propyn-1-amine, n-boc propargyl amine, prop-2-ynyl-carbamic acid tert-butyl ester | |
| DSPYCWLYGXGJNJ-UHFFFAOYSA-N | |
| tert-butyl N-prop-2-ynylcarbamate | |
| 155.197 | |
| 11073648 | |
| Moisture sensitive | |
| N-Boc-propargylamine |
Safety and Handling
GHS H Statement
H302-H315-H319-H335
Harmful if swallowed.
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
P261-P264b-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P362-P501c
H302-H315-H319-H335
TSCA : No
Recommended Storage : Keep cold; Store under Nitrogen
RUO – Research Use Only