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103788-61-0

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103788-61-0 Usage

Uses

4-Chloromethyl-5-methyl-2-phenyl-oxazole can be used for anti-tubercular activity.

Check Digit Verification of cas no

The CAS Registry Mumber 103788-61-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,7,8 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 103788-61:
(8*1)+(7*0)+(6*3)+(5*7)+(4*8)+(3*8)+(2*6)+(1*1)=130
130 % 10 = 0
So 103788-61-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H10ClNO/c1-8-10(7-12)13-11(14-8)9-5-3-2-4-6-9/h2-6H,7H2,1H3

103788-61-0SDS

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 4-(CHLOROMETHYL)-5-METHYL-2-PHENYL-1,3-OXAZOLE

1.2 Other means of identification

Product number -
Other names Chloromethyl-5-methyl-2-phenyloxazole

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:103788-61-0 SDS

103788-61-0Relevant articles and documents

New diphenylmethane derivatives as peroxisome proliferator-activated receptor alpha/gamma dual agonists endowed with anti-proliferative effects and mitochondrial activity

Piemontese, Luca,Cerchia, Carmen,Laghezza, Antonio,Ziccardi, Pamela,Sblano, Sabina,Tortorella, Paolo,Iacobazzi, Vito,Infantino, Vittoria,Convertini, Paolo,Dal Piaz, Fabrizio,Lupo, Angelo,Colantuoni, Vittorio,Lavecchia, Antonio,Loiodice, Fulvio

, p. 379 - 397 (2017)

We screened a short series of new chiral diphenylmethane derivatives and identified potent dual PPARα/γ partial agonists. As both enantiomers of the most active compound 1 displayed an unexpected similar transactivation activity, we performed docking expe

Design and synthesis of Oxime ethers of β-oxo-γ-phenylbutanoic acids as PPAR a and -γ dual agonists

Han, Hee Oon,Koh, Jong Sung,Kim, Seung Hae,Park, Ok Ku,Kim, Kyoung-Hee,Jeon, Sang Kweon,Hur, Gwong-Cheung,Yim, Hyeon Joo,Kim, Geun Tae

, p. 1979 - 1982 (2012/08/14)

Oxime ethers of p-oxo-y-phenylbutanoic acids were prepared to develop more effective PPAR a and y dual agonists. Among them, compound 11k exhibited potent in vitro activities with EC50 of 2.5 nM and 3.3 nM in PPAR a and y, respectively. It showed better g

SUBSTITUTED ACID DERIVATIVES USEFUL AS ANTIDIABETIC AND ANTIOBESITY AGENTS AND METHOD

-

Page/Page column 15-16, (2010/11/29)

Compounds are provided which have the structure of Formula (I): wherein R is hydrogen or C1-C4 alkyl; and each of R1 and R2 is independently hydrogen, C1-C4 alkyl, halo or C1-Cs

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