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67878-76-6

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67878-76-6 Usage

General Description

Methyl 5-Bromo-2-Napthoate is a chemical compound with the molecular formula C12H9BrO2. It is a derivative of naphthalene, and is commonly used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and dyes. METHYL 5-BROMO-2-NAPHTHOATE is known for its potential use in the production of anti-inflammatory and anti-cancer drugs, as well as in the manufacturing of fluorescent dyes. Methyl 5-Bromo-2-Napthoate is a versatile chemical that has a wide range of applications in the field of organic synthesis and chemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 67878-76-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,8,7 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 67878-76:
(7*6)+(6*7)+(5*8)+(4*7)+(3*8)+(2*7)+(1*6)=196
196 % 10 = 6
So 67878-76-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H9BrO2/c1-15-12(14)9-5-6-10-8(7-9)3-2-4-11(10)13/h2-7H,1H3

67878-76-6SDS

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 methyl 5-bromonaphthalene-2-carboxylate

1.2 Other means of identification

Product number -
Other names 5-bromonaphthalene-2-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:67878-76-6 SDS

67878-76-6Relevant articles and documents

N-substituted acrylamide derivatives as DHODH inhibitors and preparation and use of N-substituted acrylamide derivatives

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Paragraph 0245; 0250-0251, (2019/11/04)

The invention relates to N-substituted acrylamide derivatives as DHODH inhibitors and preparation and use of the N-substituted acrylamide derivatives. In particular, the invention discloses a compoundshown in a general formula I and the preparation and use of the compound. The compound has excellent DHODH inhibitory activation, so the compound can be used for treating or preventing various diseases caused by DHODH, the various diseases include but not limited to cancer, rheumatoid arthritis, lupus erythematosus, organ transplant rejection and other autoimmune diseases, and colitis, rhinitis and other inflammatory diseases.

Alternative and straightforward synthesis of dopaminergic 5-methoxy-1,2,3,4-tetrahydronaphthalen-2-amine

Oeztaskin, Necla,Goeksu, Sueleyman,Hasan Secen

experimental part, p. 2017 - 2024 (2011/06/24)

5-Methoxy-1,2,3,4-tetrahydronaphthalen-2-amine was synthesized from 2-naphthoic acid in six steps with an overall yield of 27%. Following the reaction sequence, bromination, esterification, substitution with NaOMe in the presence of CuI, the Birch reducti

Design and Syntheses of 1,6-Naphthalene Derivatives as Selective HCMV Protease Inhibitors

Gopalsamy, Ariamala,Lim, Kitae,Ellingboe, John W.,Mitsner, Boris,Nikitenko, Antonia,Upeslacis, Janis,Mansour, Tarek S.,Olson, Matthew W.,Bebernitz, Geraldine A.,Grinberg, Diane,Feld, Boris,Moy, Franklin J.,O'Connell, John

, p. 1893 - 1899 (2007/10/03)

Through high throughput screening of various libraries, substituted styryl naphthalene 6 was identified as an HCMV protease inhibitor. Optimization of various regions of the lead molecule using parallel synthesis resulted in 1,6-substituted naphthalenes 1

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