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4-(acetylamino)phenyl N-acetyl-DL-methionate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69217-67-0

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69217-67-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69217-67-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,2,1 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 69217-67:
(7*6)+(6*9)+(5*2)+(4*1)+(3*7)+(2*6)+(1*7)=150
150 % 10 = 0
So 69217-67-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H20N2O4S/c1-10(18)16-12-4-6-13(7-5-12)21-15(20)14(8-9-22-3)17-11(2)19/h4-7,14H,8-9H2,1-3H3,(H,16,18)(H,17,19)

69217-67-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-acetamidophenyl) (2S)-2-acetamido-4-methylsulfanylbutanoate

1.2 Other means of identification

Product number -
Other names N-acetyl-para-aminophenyl N'-acetyl-D,L-methionate

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:69217-67-0 SDS

69217-67-0Upstream product

69217-67-0Downstream Products

69217-67-0Relevant academic research and scientific papers

Analgesic N-acetyl-para-aminophenyl N'-acetylaminothioalkanoates

-

, (2008/06/13)

N-acetyl-para-aminophenyl N'-acetylaminothioalkanoates I are new analgesic compounds with greatly reduced hepatotoxic effects, when taken in overdose, relative to N-acetyl-para-aminophenol. They are prepared by reacting an N-acetylaminothioalkanoic acid IV with a reactive organic chloride V to form a mixed anhydride II and then reacting the latter with N-acetyl-para-aminophenol. The mixed anhydrides II are new and useful intermediates. Alternatively the derivatives I may be prepared by reacting the acid IV with bis-(4-nitrophenyl) sulfite to form a para-nitrophenyl N-acetylaminothioalkanoic acid ester VIII, reducing the latter to a para-aminophenyl N-acetylaminothioalkanoate VII, and acetylating this product. The esters VII and VIII are new and useful intermediates. Both reactions may pass through S-blocked intermediates, which are also new. Pharmaceutical compositions containing the derivatives I are disclosed, and also analgesic methods using them.

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