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88171-01-1

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88171-01-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88171-01-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,7 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 88171-01:
(7*8)+(6*8)+(5*1)+(4*7)+(3*1)+(2*0)+(1*1)=141
141 % 10 = 1
So 88171-01-1 is a valid CAS Registry Number.

88171-01-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl (S)-2-((tert-butoxycarbonyl)amino)-3-(1-(7-methoxy-3-oxo-2,3-dihydro-4H-benzo[b][1,4]oxazin-4-yl)-4-oxocyclohexa-2,5-dien-1-yl)propanoate

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:88171-01-1 SDS

88171-01-1Downstream Products

88171-01-1Relevant articles and documents

A multi-centered electrophile formed from a unique bioactive cyclic hydroxamic acid, 4-hydroxy-7-methoxy-2H-1,4-benzoxazin-3(4H)-one

Hashimoto, Yuichi,Ishizaki, Takayoshi,Shudo, Koichi

, p. 1837 - 1860 (2007/10/02)

4-Hydroxy-7-methoxy-2H-1,4-benzoxazin-3(4H)-one (HMBOA) is a compound of considerable interest because of its pharmacological, agrochemical, and antimicrobial properties. A plausible bioactive metabolite of HMBOA is 4-acetoxy-7-methoxy-2H-1,4-benzoxazin-3(4H)-one (AMBOA). Electrophilic reactions of AMBOA with phenols, anilines, thiols, heteroaromatics, amino acid derivatives and nucleic acids were investigated in relation to the chemical mechanisms of the biological effects elicited by the compound. The results suggest that HMBOA acts as an alkylating agent of proteins and nucleic acids in vivo after metabolic O-acylation.

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