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methyl 9-bromononanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67878-15-3

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67878-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67878-15-3 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, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 67878-15:
(7*6)+(6*7)+(5*8)+(4*7)+(3*8)+(2*1)+(1*5)=183
183 % 10 = 3
So 67878-15-3 is a valid CAS Registry Number.

67878-15-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-bromononanoic acid methyl ester

1.2 Other means of identification

Product number -
Other names 9-Brom-nonansaeure-methylester

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:67878-15-3 SDS

67878-15-3Upstream product

67878-15-3Relevant academic research and scientific papers

Studies related to in vivo C-H activation: Synthesis and influence of 8,8- and 11,11-dimethyl oleic and 11,11-dimethyl linoleic acids on Δ12- desaturation of C. sorokiniana

Poulain, Sophie,Noiret, Nicolas,Fauconnot, Laetitia,Nugier-Chauvin, Caroline,Patin, Henri

, p. 3595 - 3604 (1999)

The synthesis of three acids was achieved using the Wittig reaction in order to study their in vivo influence on the Δ12-desaturase of Chlorella sorokiniana. It was shown that the introduction of two methyls near the double bond prevent the desaturation of these exogenous acids while they seem to be accurately incorporated. This functionality could be of interest for the design of new thiaoleic acids as probes of the different oxidation processes.

DEOXYNOJIRIMYCIN DERIVATIVES AND METHODS OF THEIR USING

-

, (2016/08/29)

The present application provide novel iminosugars and their use in treatment of viral infections, such as Dengue infection and Influenza A infection. The present inventors discovered certain deoxynojirimycin derivatives may be effective against one or more viruses, which may be, for example, a Dengue virus and/or a virus belonging to the Orthomyxoviridae family, such as an Influenza A virus. In particular, such deoxynojirimycin derivatives may be useful for treating a disease or condition caused by or associated with one or more viruses. In certain embodiments, the deoxynojirimycin derivatives may increase a survival rate or probability for a subject infected with one or more viruses, which may be, for example, a Dengue virus and/or a virus belonging to the Orthomyxoviridae family, such as an Influenza A virus.

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