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192376-76-4

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192376-76-4 Usage

Uses

Methyl 3-(4-Hydroxyphenyl)benzoate acts as a reagent in the synthesis of mannoside bacterial FimH antagonists with great potentials in the treatment of urinary tract infections.

Check Digit Verification of cas no

The CAS Registry Mumber 192376-76-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,3,7 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 192376-76:
(8*1)+(7*9)+(6*2)+(5*3)+(4*7)+(3*6)+(2*7)+(1*6)=164
164 % 10 = 4
So 192376-76-4 is a valid CAS Registry Number.

192376-76-4 Well-known Company Product Price

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  • Alfa Aesar

  • (H51770)  Methyl 4'-hydroxybiphenyl-3-carboxylate, 95%   

  • 192376-76-4

  • 1g

  • 605.0CNY

  • Detail
  • Alfa Aesar

  • (H51770)  Methyl 4'-hydroxybiphenyl-3-carboxylate, 95%   

  • 192376-76-4

  • 5g

  • 2420.0CNY

  • Detail

192376-76-4SDS

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 3-(4-hydroxyphenyl)benzoate

1.2 Other means of identification

Product number -
Other names 4'-Hydroxybiphenyl-3-carboxylic acid methyl ester

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:192376-76-4 SDS

192376-76-4Relevant articles and documents

Compounds

-

, (2008/06/13)

A compound of formula I,wherein- X represents (CH2)n O, (CH2)n S or C2 alkylene;n represents 1 or 2; Ar1 represents indanyl, tetrahydronaphthyl, naphthyl or phenyl, which latter two groups may be substituted by one or more substituents selected from chloro, fluoro, OR1, O(CH2)m CONR20R21, C(O)R2, C1-6 alkyl (optionally substituted by one or more fluorine atoms), pyridyl, thiazinyl, phenyl or C7-9 alkylphenyl which latter two groups are optionally substituted by one or more substituent selected from halo, nitro, OR3, C1-6 alkyl (optionally substituted by one or more fluorine atoms), C(O)R4, C(O)OR5, C(O)N(R6)R7, CN, CH2OR14, CH2NR15R16, N(R8)R9, N(R10)SO2R11, N(R12)C(O)R13, OC(O)R19 and SO2NR17R18; m represents an integer 1 to 3; R1, R2 and R3 independently represent H, C1-10 alkyl (optionally substituted by one or more fluorine atoms), C7-9 alkylphenyl or phenyl, which latter group is optionally substituted by hydroxy; and R4, R5, R6, R7, R8, R9, R10, R11, R12, R13, R14, R15, R16, R17, R18, R19, R20 and R21 independently represent H, C1-6 alkyl (optionally substituted by one or more fluorine atoms) or phenyl; in which any alkyl group present may be interrupted by one or more oxygen atoms; provided that when X represents CH2CH2, Ar1 may not represent phenyl or phenyl substituted with one or more substituents OR1, in which R1 represents C1-10 alkyl; or a pharmaceutically acceptable derivative thereof, may be used for the treatment of a reversible obstructive airways disease or allergic conditions of the skin, nose and eye

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