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2-CHLORO-3-FLUOROBENZALDEHYDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96516-31-3

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96516-31-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96516-31-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,5,1 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 96516-31:
(7*9)+(6*6)+(5*5)+(4*1)+(3*6)+(2*3)+(1*1)=153
153 % 10 = 3
So 96516-31-3 is a valid CAS Registry Number.

96516-31-3 Well-known Company Product Price

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  • Alfa Aesar

  • (H34238)  2-Chloro-3-fluorobenzaldehyde, 95%   

  • 96516-31-3

  • 250mg

  • 461.0CNY

  • Detail
  • Alfa Aesar

  • (H34238)  2-Chloro-3-fluorobenzaldehyde, 95%   

  • 96516-31-3

  • 1g

  • 1539.0CNY

  • Detail

96516-31-3SDS

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-Chloro-3-fluorobenzaldehyde

1.2 Other means of identification

Product number -
Other names 2-CHLORO-3-FLUOROBENZALDEHYDE

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:96516-31-3 SDS

96516-31-3Relevant academic research and scientific papers

Discovery of a new 2-aminobenzhydrol template for highly potent squalene synthase inhibitors

Ichikawa, Masanori,Yokomizo, Aki,Itoh, Masao,Sugita, Kazuyuki,Usui, Hiroyuki,Shimizu, Hironari,Suzuki, Makoto,Terayama, Koji,Kanda, Akira

, p. 1930 - 1949 (2011/05/03)

To obtain small and efficient squalene synthase inhibitors, a flexible 2-aminobenzhydrol open form structure was designed and showed potent inhibitory activity comparable to 4,1-benzoxazepin compounds. Further chemical modification led to the discovery of a novel template with a strong squalene synthase inhibitory activity, and its basic structure-activity relationship was revealed. The X-ray crystallographic data of compound 12 bound to the active site of squalene synthase provided an important insight into the binding mode of this alternative template that formed 11-membered ring conformations with an intramolecular hydrogen bond.

Synthesis and antihypertensive activity of 1,4-dihydropyridine derivatives with a 4-(disubstituted phenyl) ring and an aminoalkyl ester group: Highly potent and long-lasting calcium antagonists

Kanno,Yamaguchi,Okamiya,Sunakawa,Takeshita,Naruchi

, p. 2049 - 2054 (2007/10/02)

New 1,4-dihydropyridine derivatives bearing a 4-(disubstituted phenyl) ring and an aminoethyl ester or an amino-2,2-dimethylpropyl ester were synthesized and their antihypertensive activities were examined in normotensive rats and spontaneously hypertensi

2-(2-quinazolinylaminoalkoxymethyl)-1,4-dihydropyridine derivatives as cardiovascular agents

-

, (2008/06/13)

Dihydropyridines of the formulae STR1 wherein R is chlorothienyl or mono- or disubstituted phenyl where said substituent is fluoro, chloro, bromo or trifluoromethyl; R1 and R2 are each alykl; R3 and R4 when taken separately are each hydrogen or alkyl; R3 and R4 when taken together with the nitrogen to which they are attached are piperidine or pyrrolidine; R5 is alkyl or 2-hydroxyethyl; R6 is hydrogen or methoxy; X and Z are each hydrogen or methoxy; Y is alkylene; R7 is chlorophenyl or trifluoromethyl-chlorophenyl; p is 0 or 1; and Q is CH or N are useful in the treatment of hypertension, heart failure and angina.

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