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5613-32-1

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5613-32-1 Usage

Structure

Contains a carbonyl group, a methoxy group, a chlorophenyl group, a cyclohexa-2,4-dien-1-yl moiety, and an ethanone moiety

Potential applications

Pharmaceuticals, agrochemicals, precursor for synthesis of other compounds

Properties

Reactivity with other compounds, toxicological profile, specific interactions

Complex structure

Made up of multiple functional groups

Specific content

Multiple functional groups with potential for diverse reactivity and applications

Check Digit Verification of cas no

The CAS Registry Mumber 5613-32-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,1 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5613-32:
(6*5)+(5*6)+(4*1)+(3*3)+(2*3)+(1*2)=81
81 % 10 = 1
So 5613-32-1 is a valid CAS Registry Number.

5613-32-1SDS

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 2-[6-(2-chlorobenzoyl)-3,4-dimethoxycyclohexa-2,4-dien-1-yl]-1-(4-methoxyphenyl)ethanone

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:5613-32-1 SDS

5613-32-1Relevant articles and documents

Total synthesis of synechoxanthin through iterative cross-coupling

Fujii, Seiko,Chang, Stephanie Y.,Burke, Martin D.

, p. 7862 - 7864 (2011/10/08)

The choice is yours: The first total synthesis of the antioxidant carotenoid synechoxanthin was achieved through a novel iterative cross-coupling approach in which the polarity of the bifunctional building blocks is reversed to match the preferred polarity for C-C bond formation (see scheme). The convergent, stereocontrolled, and flexible nature of this synthesis enables systematic studies of the biological activities of this natural product.

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