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84477-88-3

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84477-88-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84477-88-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,4,7 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 84477-88:
(7*8)+(6*4)+(5*4)+(4*7)+(3*7)+(2*8)+(1*8)=173
173 % 10 = 3
So 84477-88-3 is a valid CAS Registry Number.

84477-88-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Carbamic acid, N-(2-aminopropyl)-, phenylmethyl ester

1.2 Other means of identification

Product number -
Other names BENZYL2-AMINOPROPYLCARBAMATE

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:84477-88-3 SDS

84477-88-3Downstream Products

84477-88-3Relevant articles and documents

MONO carbamate protection of aliphatic diamines using alkyl phenyl carbonates [(2-Aminoethyl)carbamic acid tert-butyl ester]

Pittelkow, Michael,Lewinsky, Rasmus,Christensen, J?rn B.,Cesario, Cara,Miller, Marvin J.

, p. 209 - 214 (2017/09/07)

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Selective synthesis of carbamate protected polyamines using alkyl phenyl carbonates

Pittelkow, Michael,Lewinsky, Rasmus,Christensen, Jorn Bolstad

, p. 2195 - 2202 (2007/10/03)

Utilising alkyl phenyl carbonates, an economical, practical and versatile method for selective Boc, Cbz and Alloc protection of polyamines has been developed. This method allows Boc, Cbz and Alloc protection of primary amines in the presence of secondary amines by reaction of the polyamines with the alkyl phenyl carbonates. Also, this method allows mono carbamate protection of simple symmetrical aliphatic α,ω-alkanediamines in high yields with respect to the diamine. Finally, the method allows selective carbamate protection of a primary amine located on a primary carbon in the presence of a primary amine located on a secondary or a tertiary carbon in excellent yields.

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