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1,4-dibroMo-2-(2-broMoethoxy)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

377091-18-4

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377091-18-4 Usage

Appearance

White solid

Molecular weight

259.96 g/mol

Functional groups

Bromine atoms, ethoxy group, benzene ring

Usage

Intermediate in organic synthesis, building block for other organic compounds

Applications

Pharmaceuticals, agrochemicals, materials science

Reactivity

Versatile due to functional groups

Safety precautions

Handle with care due to potentially hazardous nature

Check Digit Verification of cas no

The CAS Registry Mumber 377091-18-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,7,0,9 and 1 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 377091-18:
(8*3)+(7*7)+(6*7)+(5*0)+(4*9)+(3*1)+(2*1)+(1*8)=164
164 % 10 = 4
So 377091-18-4 is a valid CAS Registry Number.

377091-18-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-dibromo-2-(2-bromoethoxy)benzene

1.2 Other means of identification

Product number -
Other names 2-bromoethoxy-1,4-dibromobenzene

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:377091-18-4 SDS

377091-18-4Relevant academic research and scientific papers

SPIRO COMPOUNDS AS GLYCOSIDASE INHIBITORS

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Paragraph 106; 107, (2020/03/15)

Compounds of formula (I) wherein A, R, L, Z, Q1, Q2 and n have the meaning according to the claims can be employed, inter alia, for the treatment of tauopathies and Alzheimer's disease.

TETRAHYDRO-BENZOAZEPINE GLYCOSIDASE INHIBITORS

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Page/Page column 129-130, (2020/03/15)

Compounds of formula (I') wherein A, R1, R2, T1, T2, T3, T4, L, W, Z, R''', m and n have the meaning according to the claims can be employed, inter alia, for the treatment of tauopathies and Alzheimer's disease.

FUSED GLYCOSIDASE INHIBITORS

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Page/Page column 117-118, (2020/09/08)

Compounds of formula (I), wherein A, Z, E, R1, R2, m and n have the meaning according to the claims can be employed, inter alia, for the treatment of tauopathies and Alzheimer's disease.

ANNULATED GLYCOSIDASE INHIBITORS

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Page/Page column 90, (2019/03/12)

Compounds of formula (I) wherein A, R, W1, W2, W3, W4, W5, W6, L, Q, Rx and u have the meaning according to the claims can be employed, inter alia, for the treatment of tauopathies and Alzheimer's disease.

LINEAR GLYCOSIDASE INHIBITORS

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Page/Page column 60-61, (2019/03/14)

Compounds of formula (I) wherein A, R, W, Q, L, n and m have the meaning according to the claims can be employed, inter alia, for the treatment of tauopathies and Alzheimer's disease.

5,5-DIFLUORO- AND 5-FLUORO-5-METHYL-C-GLYCOSIDE DERIVATIVES USEFUL AS DUAL SGLT1 / SGLT2 MODULATORS

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Page/Page column 95, (2019/11/28)

The present invention is directed to 5,5-difluoro- and 5-fluoro-5-methyl-C-glycoside derivatives, pharmaceutical compositions containing them and their use in the treatment of disorders and conditions modulated by SGLT activity, more particularly dual SGLT1/2 activity.

GLYCOSIDASE INHIBITORS

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Page/Page column 98, (2017/09/15)

Compounds of formula (I) wherein A, R, W, Q, n and m have the meaning according to the claims can be employed, inter alia, for the treatment of tauopathies and Alzheimer's disease.

GLYCOSIDASE INHIBITORS

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Page/Page column 83, (2017/09/15)

Compounds of formula (I) wherein A, R, W, Q, n and m have the meaning according to the claims can be employed, inter alia, for the treatment of tauopathies and Alzheimer's disease.

PROCESS FOR THE SEPARATION OF ENANTIOMERS OF PIPERAZINE DERIVATIVES

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Page/Page column 32; 34, (2017/09/21)

The invention relates to a process for preparing either enantiomer of a compound of formula (I), wherein X, Y and n have the meaning given in claim 1, with high enantiomeric excess (e.e.), by chiral resolution in the presence of a non-racemic, chiral acid.

Heterocyclic compound

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Paragraph 1107, (2016/10/08)

The present invention relates to compound (I) or a salt thereof which has a ROR γ t inhibitory action. wherein each symbol is as defined in the specification.

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