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2-(4-benzyloxycarbonylaminophenoxy)acetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

166383-74-0

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166383-74-0 Usage

Derivative of acetic acid

The compound is derived from acetic acid, which means it is structurally related to acetic acid and may share some of its properties.

Benzyl group attachment

The compound contains a benzyl group (a phenyl ring attached to a methyl group) attached to a carbonylaminophenoxy group, which influences its chemical properties and potential applications.

Carbonylaminophenoxy group

This group is a key structural component of the compound, consisting of a carbonyl group (C=O) and an amino group (NH2) attached to a phenoxy group (C6H4-O-).

Pharmaceutical industry applications

2-(4-benzyloxycarbonylaminophenoxy)acetic acid has potential applications in the pharmaceutical industry, particularly in the development of drugs for various medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 166383-74-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,3,8 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 166383-74:
(8*1)+(7*6)+(6*6)+(5*3)+(4*8)+(3*3)+(2*7)+(1*4)=160
160 % 10 = 0
So 166383-74-0 is a valid CAS Registry Number.

166383-74-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-benzyloxycarbonylaminophenoxy)acetic acid

1.2 Other means of identification

Product number -
Other names 4-(benzyloxycarbonylamino)phenoxyacetic acid

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:166383-74-0 SDS

166383-74-0Relevant academic research and scientific papers

Inhibitors of HIV protease

-

, (2008/06/13)

Compounds of formula (I): STR1 wherein: R1 is hydrogen, alkyl, aralkyl, --CORa, --CORb, --CSRa, --CSRb, --SO2 Rb, --CONHRb, --CSNHRb, --CONRb Rb or --CSNRb Rb ; R2 is hydrogen or alkyl; R3 is hydrogen, alkylidene, substituted alkyl, or Rb ; R4 is optionally substituted alkyl, cycloalkyl, or aryl; R5 is Rb O--, Rb Rb N--, Rb HN--, aralkyloxycarbonyloxy or aralkyloxycarbonylamino, or R5 is --(CH2)p --D--(CH2)r --, where D is a single bond, carbonyl, oxygen, sulfur, --NH--, --(CH2 =CH2)-- or --NHCO--; and p and r are each 0 or an integer from 1 to 5; A is --(CH2)m --B--(CH2)n -- where B is a single bond, carbonyl, oxygen, sulfur, --NH--, --(CH2 =CH2)-- or --NHCO--; and m and n are each 0 or an integer from 1 to 5; Ra is alkoxy, aralkyloxy, aryloxy or alkoxycarbonyl; Rb is optionally substituted alkyl, cycloalkyl, heterocyclic, aryl or arylalkenyl; and pharmaceutically acceptable salts and esters thereof and pro-drugs therefor, have the ability to inhibit the activity of HIV protease and may thus be used for the treatment and prophylaxis of AIDS.

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