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50670-76-3

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50670-76-3 Usage

Uses

4-(4-Ethoxycarbonylphenyl)phenol. Dyes and metabolites.

Check Digit Verification of cas no

The CAS Registry Mumber 50670-76-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,7 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 50670-76:
(7*5)+(6*0)+(5*6)+(4*7)+(3*0)+(2*7)+(1*6)=113
113 % 10 = 3
So 50670-76-3 is a valid CAS Registry Number.

50670-76-3SDS

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 ethyl 4-(4-hydroxyphenyl)benzoate

1.2 Other means of identification

Product number -
Other names ethylhydroxybiphenylcarboxylate

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:50670-76-3 SDS

50670-76-3Relevant articles and documents

Design, synthesis and biochemical evaluation of AC ring mimics as novel inhibitors of the enzyme estrone sulfatase (ES)

Ahmed, Sabbir,James, Karen,Owen, Caroline P.,Patel, Chirag K.

, p. 1343 - 1346 (2002)

We report the initial results of our study into a series of simple 4′-O-sulfamoyl-4-biphenyl based compounds as novel inhibitors of the enzyme estrone sulfatase (ES). The results of the study show that these compounds are potent inhibitors, possessing greater inhibitory activity than COUMATE, but weaker inhibitory activity than EMATE or the tricyclic derivative of COUMATE, namely 667-COUMATE. Furthermore, the compounds are observed to be irreversible inhibitors.

Iron-Catalyzed Room Temperature Cross-Couplings of Bromophenols with Aryl Grignard Reagents

Xu, Li-Chen,Liu, Kun-Ming,Duan, Xin-Fang

supporting information, p. 5421 - 5427 (2019/11/14)

Herein we report a room temperature Fe-catalyzed coupling reaction of various bromophenols with aryl Grignard reagents, which exhibits a wide substrate scope and high functional group tolerance. For the first time, the combination of simple Fe(acac)3/PBu3/Ti(OEt)4 has been used as an effective catalyst for the biaryl couplings of bromophenols or their Na or K salts with debromination and etherification side reactions being well suppressed. Various biphenols including natural product garcibiphenyl C as well as pharmaceutical diflunisal and its ethyl ester were facilely synthesized using the present protocol. (Figure presented.).

NOVEL AZO-BASED DICHROIC DYE, AND LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL ELEMENT COMPRISING THE AZO-BASED DICHROIC DYE

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Paragraph 0087; 0088; 0090, (2017/06/10)

PROBLEM TO BE SOLVED: To provide a novel azo-based dichroic dye having improved solubility with a host liquid crystal while maintaining a high order parameter (S value), and a liquid crystal composition and a liquid crystal element or the like capable of

DICHROIC DYE, LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL ELEMENT

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Paragraph 0086; 0088, (2017/07/14)

PROBLEM TO BE SOLVED: To provide a novel azo dichroic dye having solubility for practical use while maintaining high contrast order parameter (S value). SOLUTION: There is provided azo dichroic dye represented by the formula (I), where Ar1 to A1 are each independently a substituted/unsubstituted 1,4-phenylene group, a substituted/unsubstituted naphthylene group or a substituted/unsubstituted (E)-cyclohexane-1,4-diyl group, X1 is a direct bond or a bivalent group, L1 is a direct bond or a bivalent group containing no cyclic structure nor azo bond, B1 and B2 are direct bond or bivalent group containing no cyclic structure nor azo bond and Y1 and Y2 are specific general formulae. SELECTED DRAWING: Figure 1 COPYRIGHT: (C)2017,JPO&INPIT

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