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

Structure Search

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

Molecular Formula	C8H9NO2
Molecular Weight	151.1626
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

PubMed

Title	Date	PubMed
Controlled functionalization of carbon nanotubes by a solvent-free multicomponent approach.	2010-12-28	21117643
Tin(II) chloride assisted synthesis of N-protected γ-amino β-keto esters through semipinacol rearrangement.	2010-11-07	20734011
Reaction of 1,1'-divinyl ferrocene with one-electron oxidants: entry into functionalised [4]ferrocenophanes and observation of an isotope-dependent chemoselectivity effect.	2010-05-17	20391576
Stereoselective synthesis of 4-amino-2,3-unsaturated-N-Cbz-imino-O-glycosides via new diastereoisomeric N-Cbz-imino glycal-derived allyl N-nosyl aziridines.	2009-06-18	19456164
Gold(I)-catalyzed coupling reactions for the synthesis of diverse small molecules using the build/couple/pair strategy.	2009-04-22	19331418
Aziridination of C60 with simple amides and catalytic rearrangement of the aziridinofullerenes to azafulleroids.	2009-02-20	19161274
Pharmacological effects of a novel isosorbide-based butyrylcholinesterase inhibitor.	2008-09-25	18606399
HIV-1 capsid assembly inhibitor (CAI) peptide: structural preferences and delivery into human embryonic lung cells and lymphocytes.	2008-07-31	18695744
Intermolecular hydroamination of allenes with N-unsubstituted carbamates catalyzed by a gold(I) N-heterocyclic carbene complex.	2008-07-17	18570376
The reaction mechanism of the hydroamination of alkenes catalyzed by gold(I)-phosphine: the role of the counterion and the N-nucleophile substituents in the proton-transfer step.	2008-01-23	18166047
Stereoselective synthesis of 2,3-unsaturated-aza-O-glycosides via new diastereoisomeric N-Cbz-imino glycal-derived allyl epoxides.	2007-10-25	17900130
Facile synthesis of optically active imidazole derivatives.	2007-05-30	17873852
Asymmetric synthesis of N-protected chiral 1-aminoalkylphosphonic acids and synthesis of side chain-functionalized depsiphosphonopeptides.	2006-05	16285019
Facile synthesis of phosphonamidate- and phosphonate-linked phosphonopeptides.	2006-04	16245363
Synthesis of the side chain cross-linked tyrosine oligomers dityrosine, trityrosine, and pulcherosine.	2005-09-02	16122259
Efficient preparation of organic substrate-RNA conjugates via in vitro transcription.	2005-06-29	15969609
Iodine as a very powerful catalyst for three-component synthesis of protected homoallylic amines.	2004-05-28	15153045
Selective n,n-dibenzylation of primary aliphatic amines with dibenzyl carbonate in the presence of phosphonium salts.	2004-05-28	15153031
First practical protection of alpha-amino acids as N,N-benzyloxycarbamoyl derivatives.	2004-05-14	15132580
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.	2003-02-07	12558429
Preparative HPLC resolution of the CIS cyclohexane analogs of phenylalanine.	2001-01	11135415

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 19:09:58 GMT 2025` Edited by `admin` on `Mon Mar 31 19:09:58 GMT 2025`
Record UNII	7890Q001S7
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

BENZYL CARBAMATE

Systematic Name

English

NSC-25317

Preferred Name

English

PHENYLMETHYL CARBAMATE

Systematic Name

English

Code System Code Type Description

CAS

621-84-1