BENZYL CARBAMATE

Details

Stereochemistry	ACHIRAL
Molecular Formula	C8H9NO2
Molecular Weight	151.1626
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

SMILES

NC(=O)OCC1=CC=CC=C1

InChI

InChIKey=PUJDIJCNWFYVJX-UHFFFAOYSA-N

InChI=1S/C8H9NO2/c9-8(10)11-6-7-4-2-1-3-5-7/h1-5H,6H2,(H2,9,10)

HIDE SMILES / InChI

Approval Year

PubMed

Show entries

Title	Date	PubMed
Intramolecular hydrogen abstraction reaction promoted by N-radicals in carbohydrates. Synthesis of chiral 7-oxa-2-azabicyclo[2.2.1]heptane and 8-oxa-6-azabicyclo[3.2.1]octane ring systems.	2003 Feb 7	12558429
First practical protection of alpha-amino acids as N,N-benzyloxycarbamoyl derivatives.	2004 May 14	15132580
Iodine as a very powerful catalyst for three-component synthesis of protected homoallylic amines.	2004 May 28	15153045
Selective n,n-dibenzylation of primary aliphatic amines with dibenzyl carbonate in the presence of phosphonium salts.	2004 May 28	15153031
Efficient preparation of organic substrate-RNA conjugates via in vitro transcription.	2005 Jun 29	15969609

Showing 1 to 5 of 8 entries

Previous1 2Next

Patents

Show entries

Name

Type

Language

BENZYL CARBAMATE

Systematic Name

English

PHENYLMETHYL CARBAMATE

Systematic Name

English

NSC-25317

Code

English

Showing 1 to 3 of 3 entries

Previous1Next

Show entries

Code System

Code

Type

Description

CAS

621-84-1

PRIMARY

FDA UNII

7890Q001S7

PRIMARY

NSC

25317

PRIMARY

EPA CompTox

DTXSID00211159

PRIMARY

WIKIPEDIA

Benzyl carbamate

PRIMARY

Showing 1 to 5 of 7 entries

Previous1 2Next

SUBSTANCE RECORD


					7890Q001S7

BENZYL CARBAMATE