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Benzoic acid, 5-amino-2-(6-hydroxy-3-oxo-3H-xanthen-9-yl)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

313376-39-5

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313376-39-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 313376-39-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,3,3,7 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 313376-39:
(8*3)+(7*1)+(6*3)+(5*3)+(4*7)+(3*6)+(2*3)+(1*9)=125
125 % 10 = 5
So 313376-39-5 is a valid CAS Registry Number.

313376-39-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 5-amino-2-(3-hydroxy-6-oxoxanthen-9-yl)benzoate

1.2 Other means of identification

Product number -
Other names -

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:313376-39-5 SDS

313376-39-5Upstream product

313376-39-5Relevant academic research and scientific papers

Fluorescein-based compounds and their use for peptide synthesis

-

, (2008/06/13)

The present invention is related to new fluorescein derivatives, the method for producing such derivatives and their use for the synthesis of fluorogenic peptides and in particular protease substrates and peptide ligands.

Fluorescein-based amino acids for solid phase synthesis of fluorogenic protease substrates

Burchak, Olga N.,Mugherli, Laurent,Chatelain, Francois,Balakirev, Maxim Y.

, p. 2559 - 2568 (2007/10/03)

An efficient synthesis of new type fluorescent amino acids is described. The Fmoc-protected dyes can be prepared in a four-step procedure with ~30% overall yield from aminofluoresceins and other inexpensive commercially available precursors. The dyes are

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