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133554-24-2

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133554-24-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133554-24-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,5,5 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 133554-24:
(8*1)+(7*3)+(6*3)+(5*5)+(4*5)+(3*4)+(2*2)+(1*4)=112
112 % 10 = 2
So 133554-24-2 is a valid CAS Registry Number.

133554-24-2SDS

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 methyl 4-(6-hydroxy-5-nitro-1,3-benzoxazol-2-yl)benzoate

1.2 Other means of identification

Product number -
Other names -

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:133554-24-2 SDS

133554-24-2Downstream Products

133554-24-2Relevant articles and documents

4 - [6 - (methylthio) benzo [1,2-d:5,4-d '] b [1,3] oxazole-2-yl] benzoic acid and its preparation method

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Paragraph 0034-0036, (2017/02/28)

The invention discloses 4-[6-(methylthio) benzo [1, 2-d: 5, 4-d']-di-[1, 3] oxaxole-2-yl] benzoic acid and a preparation method thereof. The preparation method comprises the steps as follows: resorcinol is taken as a raw material and subjected to sulfonation, nitration, hydrolysis and reduction to obtain 4-amino-6-nitroresorcinol hydrochloride; ANR*HCl and p-methoxycarbonyl benzoyl chloride (MBC) are subjected to condensation, cyclization and dehydration to obtain 4-(6-hydroxy-5-nitrobenzo[d]oxazole-2-yl) methyl benzoate; NHABE is subjected to hydrogenation reduction under the action of a Pd/C catalyst to obtain 4-(6-hydroxy-5-aminobenzo[d]oxazole-2-yl) methyl benzoate; AHABE and CS2 are subjected to cyclization under the alkaline condition to obtain 4-(6-(mercapto)benzo[1, 2-d:5, 4-d']-di-(oxazole)-2-yl) benzoic acid; and dimethyl methyl sulfate is compounded to the target compound 4-[6-(methylthio) benzo [1, 2-d: 5, 4-d']-di-[1, 3] oxaxole-2-yl] benzoic acid. According to the invention, a novel compound is obtained, the method is simple and convenient, and the product yield is high.

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