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29669-49-6

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29669-49-6 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 36, p. 2188, 1971 DOI: 10.1021/jo00814a036

Check Digit Verification of cas no

The CAS Registry Mumber 29669-49-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,6,6 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 29669-49:
(7*2)+(6*9)+(5*6)+(4*6)+(3*9)+(2*4)+(1*9)=166
166 % 10 = 6
So 29669-49-6 is a valid CAS Registry Number.

29669-49-6SDS

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 5-fluorothiophene-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names 5-fluoro-2-thiophenecarbaldehyde

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:29669-49-6 SDS

29669-49-6Relevant articles and documents

METHODS OF TREATING PULMONARY DISEASES AND DISORDERS

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, (2017/07/14)

The present disclosure features disclosed method of treating disorders such as COPD, bronchitis and/or asthma using disclosed compounds, optionally together with one or more additional active agents. Contemplated methods include administrating orally or by inhalation to a patient one or more disclosed compounds.

FLUORO-SUBSTITUTED INHIBITORS OF D-AMINO ACID OXIDASE

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Page/Page column 31, (2008/06/13)

This invention provides novel inhibitors of the enzyme D-amino acid oxidase as well as pharmaceutical compositions including the compounds of the invention. The invention also provides methods for the treatment and prevention of neurological disorders, such as neuropsychiatric and neurodegenerative diseases, as well as pain, ataxia and convulsion. The compounds of the invention have the general structure: wherein A is NH or S. Q is a member selected from CR1 and N. X and Y are members independently selected from O, S, CR2, N and NH. R1, R2 and R4 are members independently selected from H and F, provided that at least one member selected from R1, R2 and R4 is F. R6 is a member selected from O?X+ and OH, wherein X+ is a positive ion, which is a member selected from inorganic positive ions and organic positive ions.

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