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66727-64-8

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66727-64-8 Usage

General Description

ASISCHEM W99822 is a chemical compound that is commonly known as 3-Methoxycinnamic Acid. It is a white crystalline powder that is used as a flavoring agent in the food industry and as an intermediate in the synthesis of various pharmaceuticals. It is also used in the production of fragrances and in the manufacturing of dyes and pigments. ASISCHEM W99822 has been reported to have anti-inflammatory and antioxidant properties, making it a valuable compound for use in medicinal applications. Additionally, it is used in the production of sunscreen and other cosmetic products due to its ability to absorb UVB radiation.

Check Digit Verification of cas no

The CAS Registry Mumber 66727-64-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,7,2 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 66727-64:
(7*6)+(6*6)+(5*7)+(4*2)+(3*7)+(2*6)+(1*4)=158
158 % 10 = 8
So 66727-64-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H13NO/c1-3-13-9(2)11(8-14)10-6-4-5-7-12(10)13/h4-8H,3H2,1-2H3

66727-64-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethyl-2-methylindole-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 1-ethyl-3-formyl-2-methylindole

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:66727-64-8 SDS

66727-64-8Relevant articles and documents

Selective nickel-catalyzed dehydrogenative-decarboxylative formylation of indoles with glyoxylic acid

Yin, Zhiping,Wang, Zechao,Wu, Xiao-Feng

supporting information, p. 3707 - 3710 (2018/05/31)

Herein we present a new strategy for the dehydrogenative-decarboxylative coupling of indoles with glyoxylic acid. A broad range of indoles were transformed into the corresponding 3-formylindoles in moderate to good yields and excellent functional group tolerance. Notably, no N-formylation product was detected under our conditions.

Novel compounds, processes and marking systems

-

, (2008/06/13)

Mono and bis substituted (arylsulfonyl)alkanes useful as color formers, particularly in carbonless duplicating and thermal marking systems, are prepared by the interaction of the appropriate aldehyde or dialdehyde with the appropriate aryl or heterocyclic moiety and the appropriate phenylsulfinic acid in the presence of a catalyst.

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