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4702-37-8

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4702-37-8 Usage

Derivative of

Coumarin

Uses

Production of pharmaceuticals and perfumes, fragrance and flavoring agent

Odor

Distinct sweet, hay-like

Therapeutic properties

Anti-coagulant and antioxidant effects

Toxicity

Associated with certain toxic effects when ingested in large quantities

Regulation

Use in consumer products is regulated in some regions.

Check Digit Verification of cas no

The CAS Registry Mumber 4702-37-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,0 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4702-37:
(6*4)+(5*7)+(4*0)+(3*2)+(2*3)+(1*7)=78
78 % 10 = 8
So 4702-37-8 is a valid CAS Registry Number.

4702-37-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name isochromene-1-thione

1.2 Other means of identification

Product number -
Other names 1-Thio-isocumarin

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:4702-37-8 SDS

4702-37-8Upstream product

4702-37-8Downstream Products

4702-37-8Relevant articles and documents

EPR studies on carboxylic esters. Part 20. EPR spectra and spin densities in radical anions of isocoumarin, benzocoumarin and their sulfur analogues

Voss, Juergen,Kupczik, Gabriele,Stahncke, Heidi

experimental part, p. 283 - 286 (2009/12/07)

The radical anions of isocoumarin, benzocoumarin and the six corresponding sulfur analogues have been generated by internal electroreduction and studied by EPR spectrosopy. The spin density distributions have been evaluated from the proton hyperfine structure coupling constants and by MO calculations. They are discussed with respect to the spin density distributions in related radical anions.

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