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683215-19-2

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683215-19-2 Usage

Structure

A derivative of malonic acid with a 3-chlorobenzyl group attached

Appearance

White to off-white crystalline solid

Solubility

Slightly soluble in water

Applications

Organic synthesis, pharmaceutical research, building block for organic compound synthesis, precursor for pharmaceutical drug production, potential biological activities for drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 683215-19-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,3,2,1 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 683215-19:
(8*6)+(7*8)+(6*3)+(5*2)+(4*1)+(3*5)+(2*1)+(1*9)=162
162 % 10 = 2
So 683215-19-2 is a valid CAS Registry Number.

683215-19-2SDS

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-(3-chlorobenzyl)malonic acid

1.2 Other means of identification

Product number -
Other names (3-Chlor-benzyl)-malonsaeure

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:683215-19-2 SDS

683215-19-2Relevant articles and documents

Synthesis and insecticidal activity of mesoionic pyrido[1,2-α]pyrimidinone derivatives containing a neonicotinoid moiety

Pan, Jianke,Yu, Lu,Liu, Dengyue,Hu, Deyu

, (2018/05/30)

Mesoionic pyrido[1,2-α]pyrimidinone derivatives containing a neonicotinoid moiety were designed, synthesized, and evaluated for their insecticidal activity. Some of the title compounds showed remarkable insecticidal properties against Aphis craccivora. Compound I13 exhibited satisfactory insecticidal activity against A. craccivora. Meanwhile, label-free proteomics analysis of compound I13 treatment identified a total of 821 proteins. Of these, 35 proteins were up-regulated, whereas 108 proteins were down-regulated. Differential expressions of these proteins reflected a change in cellular structure and metabolism.

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