BOC-GLY-NH2
- CAS NO.:35150-09-5
- Empirical Formula: C7H14N2O3
- Molecular Weight: 174.2
- MDL number: MFCD08275106
- EINECS: 1533716-785-6
- SAFETY DATA SHEET (SDS)
- Update Date: 2024-08-11 15:28:25
What is BOC-GLY-NH2?
The Uses of BOC-GLY-NH2
Boc-Glycinamide is a useful synthetic intermediate. It is used to prepare primary amides as selective inhibitors of cathepsin K. It is also used to prepare group A streptococcal vaccine.
Properties of BOC-GLY-NH2
Melting point: | 85-87 °C |
Boiling point: | 339.7±25.0 °C(Predicted) |
Density | 1.107±0.06 g/cm3(Predicted) |
storage temp. | Sealed in dry,Store in freezer, under -20°C |
pka | 12.01±0.46(Predicted) |
form | Solid |
color | White |
Safety information for BOC-GLY-NH2
Signal word | Warning |
Pictogram(s) |
Exclamation Mark Irritant GHS07 |
GHS Hazard Statements |
H302:Acute toxicity,oral H315:Skin corrosion/irritation H319:Serious eye damage/eye irritation H335:Specific target organ toxicity, single exposure;Respiratory tract irritation |
Precautionary Statement Codes |
P261:Avoid breathing dust/fume/gas/mist/vapours/spray. P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing. |
Computed Descriptors for BOC-GLY-NH2
New Products
4-Aminotetrahydropyran-4-carbonitrile Hydrochloride (R)-3-Aminobutanenitrile Hydrochloride 4-AMINO-TETRAHYDRO-PYRAN-4-CARBOXYLIC ACID HCL 4-(Dimethylamino)tetrahydro-2H-pyran-4-carbonitrile 3-((Dimethylamino)methyl)-5-methylhexan-2-one oxalate 1,4-Dioxa-8-azaspiro[4.5]decane 5-Bromo-2-nitropyridine Nimesulide BP Aceclofenac IP/BP/EP Mefenamic Acid IP/BP/EP/USP Diclofenac Sodium IP/BP/EP/USP Ornidazole IP Diclofenac Potassium SODIUM AAS SOLUTION ZINC AAS SOLUTION BUFFER SOLUTION PH 10.0(BORATE) GOOCH CRUCIBLE SINTERED AQUANIL 5 BERYLLIUM AAS SOLUTION 2-Bromo-1-(bromomethyl)-3-chloro-5-nitrobenzene 2-Bromo-3-nitroaniline N-(3-Hydroxypropyl)-N-methylacetamide 3-Bromo-6-chloropyridazine 4-ethyl-3-nitrobenzoic acidRelated products of tetrahydrofuran
Carbamic acid, (phenylsulfonyl)-, 1,1-dimethylethyl ester
tert-butyl N-[(1s,3s)-3-{[imino(methyl)oxo-lambda6-sulfanyl]methyl}cyclobutyl]carbamate, cis
tert-butyl N-[(1R)-1-cyclohexylethyl]carbamate
(3S)-3-(tert-Butoxycarbonyl)amino-1-chloro-4-phenyl-2-butanone
TERT-BUTYL N-(6-HYDROXYHEXYL)CARBAMATE
tert-butyl N-[(2S)-5-bromo-4-oxopentan-2-yl]carbamate
tert-butyl N-[(2R,3S)-3-aminobutan-2-yl]carbamate hydrochloride
(S)-(2-Amino-3,3-dimethyl-butyl)-carbamic acid tert-butyl ester
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