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146137-80-6

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146137-80-6 Usage

Chemical Properties

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Check Digit Verification of cas no

The CAS Registry Mumber 146137-80-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,1,3 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 146137-80:
(8*1)+(7*4)+(6*6)+(5*1)+(4*3)+(3*7)+(2*8)+(1*0)=126
126 % 10 = 6
So 146137-80-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H7F3O2S/c1-16-10(15)9-5-6-7(11(12,13)14)3-2-4-8(6)17-9/h2-5H,1H3

146137-80-6 Well-known Company Product Price

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  • Alfa Aesar

  • (H26626)  2-Fluoro-4-methylbenzaldehyde, 97%   

  • 146137-80-6

  • 1g

  • 1559.0CNY

  • Detail
  • Alfa Aesar

  • (H26626)  2-Fluoro-4-methylbenzaldehyde, 97%   

  • 146137-80-6

  • 5g

  • 4769.0CNY

  • Detail

146137-80-6SDS

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-Fluoro-4-methylbenzaldehyde

1.2 Other means of identification

Product number -
Other names 2-fluoro-4-methybenzaldehyde

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:146137-80-6 SDS

146137-80-6Relevant articles and documents

Loxoprofen derivative

-

Paragraph 0035-0036; 0038, (2019/01/23)

The invention provides a Loxoprofen derivative. Gastrointestinal tract side effects are low, and the bioavailability can be improved.

Properties and synthesis of 2-{2-fluoro (or bromo)-4-[(2-oxocyclopentyl) methyl]phenyl}propanoic acid: Nonsteroidal anti-inflammatory drugs with low membrane permeabilizing and gastric lesion-producing activities

Yamakawa, Naoki,Suemasu, Shintaro,Matoyama, Masaaki,Kimoto, Ayumi,Takeda, Miho,Tanaka, Ken-Ichiro,Ishihara, Tomoaki,Katsu, Takashi,Okamoto, Yoshinari,Otsuka, Masami,Mizushima, Tohru

scheme or table, p. 7879 - 7882 (2011/02/22)

We previously proposed that membrane permeabilization activity of NSAIDs is involved in NSAID-induced gastric lesions. We here synthesized derivatives of loxoprofen that have lower membrane permeabilization activity than other NSAIDs. Compared to loxoprofen, the derivatives 10a and 10b have lower membrane permeabilization activity and their oral administration produced fewer gastric lesions but showed an equivalent anti-inflammatory effect. These results suggest that 10a and 10b are likely to be therapeutically beneficial as safer NSAIDs.

Pyrazolopyrimidines as therapeutic agents

-

, (2008/06/13)

The present invention is directed to pyrazolopyrimidine derivatives of formula (I) wherein the substituents are defined herein, which are useful as kinase inhibitors and as such are useful for affecting angiogenesis and diseases and conditions associated with angiogenesis.

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