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882847-15-6

882847-15-6

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882847-15-6 Usage

Uses

Fmoc-(2-aminomethylphenyl)acetic acid

Check Digit Verification of cas no

The CAS Registry Mumber 882847-15-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,2,8,4 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 882847-15:
(8*8)+(7*8)+(6*2)+(5*8)+(4*4)+(3*7)+(2*1)+(1*5)=216
216 % 10 = 6
So 882847-15-6 is a valid CAS Registry Number.

882847-15-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-(aminomethyl)phenyl]-3-(9H-fluoren-9-ylmethoxy)-3-oxopropanoic acid

1.2 Other means of identification

Product number -
Other names FMOC-2-AMINOMETHYL-PHENYLACETIC 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:882847-15-6 SDS

882847-15-6Downstream Products

882847-15-6Relevant articles and documents

COMPOUNDS AND USES THEREOF

-

Page/Page column 53, (2020/06/10)

The present invention features compounds useful in the treatment of adenosine or adenosine receptor related disorders.

Preparation of amides from acids and resin bound azides: Suppression of intramolecular lactam formation

Tang, Zhilian,Pelletier, Jeffrey C.

, p. 4773 - 4776 (2007/10/03)

A new method for the formation of amides on solid phase has been developed. The procedure involves the reaction between activated acids in solution and resin bound iminophosphoranes generated from the corresponding azides and tributylphosphine. The method is particularly attractive when starting from δ azido acids since amides can form without internal cyclization to the lactam.

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