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83324-59-8

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83324-59-8 Usage

Uses

3-chloro-4,6-dihydroxy-2-methylbenzaldehyde is a lichen/fungal metabolite.

Check Digit Verification of cas no

The CAS Registry Mumber 83324-59-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,3,2 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 83324-59:
(7*8)+(6*3)+(5*3)+(4*2)+(3*4)+(2*5)+(1*9)=128
128 % 10 = 8
So 83324-59-8 is a valid CAS Registry Number.

83324-59-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chloro-4,6-dihydroxy-2-methylbenzaldehyde

1.2 Other means of identification

Product number -
Other names 3-chloro-4,6-dihydroxy-2-methyl-benzaldehyde

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:83324-59-8 SDS

83324-59-8Relevant articles and documents

COMPOUNDS FOR USE AS INHIBITORS OF ALTERNATIVE OXIDASE OR CYTOCHROME BC1 COMPLEX

-

, (2015/07/27)

The invention provides compounds for use in inhibiting a microbial alternative oxidase (AOX) and/or cytochrome bc1 complex. The invention extends to the use of such inhibitors in agrochemicals and in pharmaceuticals, for treating microbial infe

Synthetic study for two 2H-chromenic acids, 8-chlorocannabiorcichromenic acid and mycochromenic acid

Yamaguchi, Seiji,Nedachi, Masahiro,Maekawa, Mikiko,Murayama, Yohei,Miyazawa, Masahiro,Hirai, Yoshiro

, p. 29 - 41 (2007/10/03)

Two 2H-chromenes having a fully substituted benzene ring, 8-chlorocannabioreichromene (1) and mycochromenic acid (2), were synthesized by a condensation of salicylaldehydes with isopropylidenemalonate or the thermal cyclization of corresponding propargyl ethers.

A CONVENIENT SYNTHESIS OF (+/-) ASCOCHLORIN

Safaryn, J. E.,Chiarello, J.,Chen, K.-M.,Joullie, M. M.

, p. 2635 - 2642 (2007/10/02)

A convergent total synthesis of (+/-) ascochlorin is described.

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