BOC- Gly- Ome
Also known as N-Boc-glycine Methyl Ester, N-(tert-Butoxycarbonyl)glycine methyl ester, methyl 2-[(2-methylpropan-2-yl)oxycarbonylamino]acetate
- CAS number
- 31954-27-5
- Molecular formula
- C8H15NO4
- Molecular weight
- 189.21 g/mol
- Catalogue number
- OS-18587
- Purity
- 99 %
- Grade
- Pharmaceutical (IP/BP/USP/EP)
- Form
- Powder
- Packing
- 25 kg
₹3,000 per kg
Documents
- Certificate of analysis (COA) On request
- Safety data sheet (MSDS) On request
Specifications
| CAS number | 31954-27-5 |
|---|---|
| Molecular formula | C8H15NO4 |
| Molecular weight | 189.21 g/mol |
| IUPAC name | methyl 2-[(2-methylpropan-2-yl)oxycarbonylamino]acetate |
| InChIKey | PHUZOEOLWIHIKH-UHFFFAOYSA-N |
| SMILES | CC(C)(C)OC(=O)NCC(=O)OC |
| MDL number | MFCD00038267 |
| PubChem CID | 637609 |
| Physical form | Powder |
|---|
| Purity | 99 % |
|---|---|
| Grade | Pharmaceutical (IP/BP/USP/EP) |
| Packaging size | 25 kg |
|---|
Description and applications
Synonums:
Boc-glycine methyl esterBoc-glycine methyl ester is a versatile compound widely utilized in peptide synthesis and organic chemistry. This protected amino acid derivative features a tert-butyloxycarbonyl (Boc) group, which provides stability and enhances the compound's reactivity during various chemical reactions. Its unique structure allows for selective deprotection, making it an essential building block in the synthesis of complex peptides and pharmaceuticals. Researchers and industry professionals appreciate its role in facilitating the formation of peptide bonds while maintaining the integrity of sensitive functional groups.
Boc-glycine methyl esterBoc-glycine methyl ester is a versatile compound widely utilized in peptide synthesis and organic chemistry. This protected amino acid derivative features a tert-butyloxycarbonyl (Boc) group, which provides stability and enhances the compound's reactivity during various chemical reactions. Its unique structure allows for selective deprotection, making it an essential building block in the synthesis of complex peptides and pharmaceuticals. Researchers and industry professionals appreciate its role in facilitating the formation of peptide bonds while maintaining the integrity of sensitive functional groups.
Applications
- Protected amino acid
More protected amino acids
All 21 protected amino acids-
BOC-D- Phenyl glycine
(2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid, Boc-D-Phg-OH
CAS 33125-05-2 C13H17NO4 99 % -
N-BOC-D- Phenyl glycinol
1,1-Dimethylethyl N-((1R)-2-hydroxy-1-phenylethyl)carbamate, (R)-N-(tert-Butoxycarbonyl)-2-phenylglycinol
CAS 102089-74-7 C13H19NO3 99 % -
Boc- Gly- OH
N-(tert-Butoxycarbonyl)glycine, N-Boc-glycine
CAS 4530-20-5 C7H13NO4 98 % -
Boc- L- Alanine
tert-butoxycarbonylalanine, t-BA amino acid
CAS 15761-38-3 C8H15NO4 99 % -
N-BOC-L- Hydroxy proline
Boc-Hyp-OH, N-Boc-trans-4-hydroxy-L-proline
CAS 13726-69-7 C10H17NO5 7 % -
N-BOC-L- phenyl alanine
N-(tert-Butoxycarbonyl)-L-phenylalanine, N-t-Butyloxycarbonyl-L-phenylalanine
CAS 13734-34-4 C14H19NO4 99 %
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