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108327-31-7

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108327-31-7 Usage

Molecular structure

Contains a naphthalene ring and a carbamic acid ester group.

Industry usage

Often used in the pharmaceutical industry.

Medical applications

Used as an intermediate or precursor in the synthesis of pharmaceuticals, including antihypertensive and anti-inflammatory drugs.

Chemical research

Used as a reagent in chemical research.

Synthesis building block

Used as a building block for the synthesis of other complex organic compounds.

Versatility

1-Naphthalenepropanoic acid, a-[[(phenylmethoxy)carbonyl]amino]is a versatile and important chemical compound with various practical applications in the field of medicine and research.

Check Digit Verification of cas no

The CAS Registry Mumber 108327-31-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,3,2 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 108327-31:
(8*1)+(7*0)+(6*8)+(5*3)+(4*2)+(3*7)+(2*3)+(1*1)=107
107 % 10 = 7
So 108327-31-7 is a valid CAS Registry Number.

108327-31-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name α-(((Phenylmethoxy)carbonyl)amino)-1-naphthalenepropanoic acid

1.2 Other means of identification

Product number -
Other names 2-benzyloxycarbonylamino-3-[1]naphthyl-propionic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:108327-31-7 SDS

108327-31-7Relevant articles and documents

Studies on Cyclic Dipeptides, I: Aryl Modifications of cyclo-[Phe-His]

Noe,Weigand,Pirker

, p. 1081 - 1097 (1996)

Seven new cyclic dipeptides have been synthesized and tested for their applicability as tools to elucidate the mechanism of formation of mandelonitrile with (SS)-cyclo-[Phe-His] type catalysts. Conformational analyses based on 1H NMR spectra are presented for all prepared cyclic dipeptides.

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