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Benzyl carbamate

Benzyl carbamate Structure
CAS No.
621-84-1
Chemical Name:
Benzyl carbamate
Synonyms
Z-NH2;CARBAM;O-Benzylcarbamate;Benzyl aminoformate;N-CARBOBENZOXY-AMIDE;CarbaMyl Benzyl Ester;CARBAMIC ACID BENZYL ESTER;Z-AMIDE;Benzyl urethane;BENZYL CARBAMATE
CBNumber:
CB5100170
Molecular Formula:
C8H9NO2
Molecular Weight:
151.16
MOL File:
621-84-1.mol
MSDS File:
SDS
Modify Date:
2024/7/29 17:07:33

Benzyl carbamate Properties

Melting point 86-89 °C (lit.)
Boiling point 273.17°C (rough estimate)
Density 1.2023 (rough estimate)
refractive index 1.5810 (estimate)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Chloroform (Slightly), Methanol (Slightly)
pka 13.42±0.50(Predicted)
form Powder or Flakes
color Off-white to light beige
Water Solubility 68.02g/L(37 ºC)
BRN 1865635
InChIKey PUJDIJCNWFYVJX-UHFFFAOYSA-N
CAS DataBase Reference 621-84-1(CAS DataBase Reference)
NIST Chemistry Reference Carbamic acid, benzyl ester(621-84-1)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P271-P280
Hazard Codes  Xn
Risk Statements  20/21/22-36/37/38
Safety Statements  22-24/25-36-26
WGK Germany  3
HS Code  29242995
NFPA 704
1
2 0

Benzyl carbamate price More Price(4)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) B18200 Benzyl carbamate 99% 621-84-1 25G ₹2381.5 2022-06-14 Buy
Sigma-Aldrich(India) B18200 Benzyl carbamate 99% 621-84-1 100G ₹6949.65 2022-06-14 Buy
TCI Chemicals (India) C0590 Benzyl Carbamate 621-84-1 25G ₹3200 2022-05-26 Buy
TCI Chemicals (India) C0590 Benzyl Carbamate 621-84-1 250G ₹13900 2022-05-26 Buy
Product number Packaging Price Buy
B18200 25G ₹2381.5 Buy
B18200 100G ₹6949.65 Buy
C0590 25G ₹3200 Buy
C0590 250G ₹13900 Buy

Benzyl carbamate Chemical Properties,Uses,Production

Chemical Properties

Off-white to light beige powder or flakes, melting point 87-89 ℃. Insoluble in water, soluble in organic solvents such as benzene.

Uses

Benzyl carbamate is a reagent used for the nucleophilic introduction of an amino-protected group, Benzyl carbamates can be considered as a benzyloxycarbonyl (otherwise known as carbobenzyloxy, Cbz or Z) protecting group for amino groups. It was introduced as a versatile alternative to the ethoxy carbamate group in peptide synthesis.

Application

Benzyl carbamate is an intermediate in the synthesis of various pharmaceutical compounds. It can be also used as nondeuterated internal standards for the quantitative analysis of carisoprodol in blood.

Preparation

Benzyl carbamate is prepared by reacting benzyl chloroformate with ammonia. Benzyl chloroformate was slowly added to 5 times the volume of cold ammonia water (relative density 0.90) under vigorous stirring, the reaction mixture was placed at room temperature for 30 minutes, the precipitate was filtered out, washed with water and dried to obtain the finished product of benzyl carbamate.

Purification Methods

If it smells of NH3, then dry it in a vacuum desiccator and recrystallise it from 2 volumes of toluene and dry it in a vacuum desiccator again. It forms glistening plates from toluene, and can be recrystallised from H2O [Martell & Herbst J Org Chem 6 878 1941, Carter et al. Org Synth Coll Vol III 168 1955]. [Beilstein 6 IV 2278.]

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Z-AMIDE BENZYLOXYCARBONYL AMIDE BENZYL CARBAMATE Benzylcarbamate (Z-NH2) Carbamic acid benzyl ester~Z-NH_2 Benzyl carbamate,98% Phenylmethyl carbamate Benzyl urethane Benzyloxycarbonylamine Benzyl carbaMate, 98% 25GR Z-NH2 Benzyl carbamate Benzyl carbaMate 99% Carbobenzoxyamide Benzylcarbamate(BC) TIANFUCHEM--621-84-1--Benzyl carbamate factory price Benzyl Carbamate > Benzyl carbamate ISO 9001:2015 REACH N-CARBOBENZOXY-AMIDE O-Benzylcarbamate Z-NH2 CARBAMIC ACID BENZYL ESTER CARBAM Benzyl aminoformate CarbaMyl Benzyl Ester 621-84-1 H2NCOOCH2C6H5 NH2COOCH2C6H5 H2NCO2CH2C6H5 Protected Amines Nitrogen Compounds Organic Building Blocks Building Blocks Building Blocks Chemical Synthesis Nitrogen Compounds Organic Building Blocks Protected Amines Heterocycles Nitrogen Compounds Organic Building Blocks Protected Amines bc0001