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5-((2-(2-naphthalenylmethyl)-5-benzoxazolyl)methyl)-2,4-thiazolidinedione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

118384-10-4

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118384-10-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118384-10-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,3,8 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 118384-10:
(8*1)+(7*1)+(6*8)+(5*3)+(4*8)+(3*4)+(2*1)+(1*0)=124
124 % 10 = 4
So 118384-10-4 is a valid CAS Registry Number.
InChI:InChI=1/C22H16N2O3S/c25-21-19(28-22(26)24-21)11-14-6-8-18-17(10-14)23-20(27-18)12-13-5-7-15-3-1-2-4-16(15)9-13/h1-10,19H,11-12H2,(H,24,25,26)

118384-10-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[[2-(naphthalen-2-ylmethyl)-1,3-benzoxazol-5-yl]methyl]-1,3-thiazolidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 5-Nmebontd

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:118384-10-4 SDS

118384-10-4Downstream Products

118384-10-4Relevant academic research and scientific papers

Novel benzoxazole 2,4-thiazolidinediones as potent hypoglycemic agents. Synthesis and structure-activity relationships

Arakawa, Kenji,Inamasu, Masanori,Matsumoto, Mamoru,Okumura, Kunihito,Yasuda, Kosuke,Akatsuka, Hidenori,Kawanami, Saburo,Watanabe, Akishige,Homma, Koichi,Saiga, Yutaka,Ozeki, Masakatsu,Iijima, Ikuo

, p. 1984 - 1993 (1997)

A new series of benzoxazole 2,4-thiazolidinediones was synthesized and evaluated for hypoglycemic activity in genetically obese and diabetic yellow KK mice. 2-Arylmethyl- and 2-(heteroarylmethyl)benzoxazole derivatives showed far more potent activity than known 2,4-thiazolidinedione derivatives such as ciglitazone, troglitazone and pioglitazone. A facile synthesis of benzoxazole 2,4-thiazolidinediones was also established using aminophenol 2,4- thiazolidinedione (11) as a key intermediate. Details of synthesis and structure-activity relationships for this series are described.

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