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6-butanoyl-1,3-benzoxazol-2(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70735-85-2

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70735-85-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70735-85-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,7,3 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 70735-85:
(7*7)+(6*0)+(5*7)+(4*3)+(3*5)+(2*8)+(1*5)=132
132 % 10 = 2
So 70735-85-2 is a valid CAS Registry Number.

70735-85-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-butanoyl-3H-1,3-benzoxazol-2-one

1.2 Other means of identification

Product number -
Other names 6-butanoyl-2(3H)benzoxazolone

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:70735-85-2 SDS

70735-85-2Relevant academic research and scientific papers

A Convenient and Efficient Method for the Preparation of 6-Acyl-2(3H)-benzoxazolones

Aichaoui, Hocine,Lesieur, Daniel,Henichart, Jean-Pierre

, p. 171 - 175 (2007/10/02)

Benzoxazolinone derivatives have been found to exhibit various pharmacological properties and 6-acyl-2(3H)-benzoxazolones are considered as key starting materials for the preparation of these compounds.Reported here are the optimal conditions for a regioselective acylation at the 6-position of the benzoxazolinone ring.A general method leading to the expected products in excellent yields consists in using a mixture of aluminum chloride-dimethylformamide as catalyst and acid anhydrides or chlorides as acylating agents.

ACYLATION OF 2,3-DIHYDROBENZOXAZOL-2-ONE IN A TWO STEPS METHOD INVOLVING AN ACYL MIGRATION

Cotelle, Nicole,Cotelle, Philippe,Lesieur, Daniel

, p. 3259 - 3266 (2007/10/02)

A new method of acylation of 2,3-dihydrobenzoxazol-2-one 1 is proposed in a two-steps procedure involving an acyl migration.

Acyl-7 dihydro-2,3 benzoxazin-1,4 ones-3 et proprietes normolipemiantes

Moussavi, Ziaeddine,Lesieur, Daniel,Lespagnol, Charles,Sauzieres, Jacques,Olivier, Philippe

, p. 55 - 60 (2007/10/02)

7-Acyl-2,3-dihydro-1,4-benzoxazin-3-ones and normolipemic properties.Fibrates are still among the most widely used drugs for the treatment of dyslipoproteinemia. 7-Acyl-2,3-dihydro-1,4-benzoxazin-3-ones (Fig.1B) can be considered as conformationally restrained analogues of fibrates, such as fenofibrate.These compounds have been prepared and studied for their normolipemic activity particularly on plasma cholesterol, triglyceride and high density lipoprotein (HDL) cholesterol levels.Hepatotoxicity and mutagenicity have also been evaluated.Some of them show an interesting activity, quite comparable to fenofibrate, and are devoid of hepatotoxicity. hyperlipidemia / hypocholesterolemic drugs / fibrates / 7-acyl-1,4-benzoxazin-3-ones

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