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395-07-3

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395-07-3 Usage

Functional Groups

Fluoro-substituted phenyl group, 1,2-dione 2-oxime

Usage

Organic synthesis, pharmaceutical research

Potential Applications

Development of new drugs, building block for synthesis of other organic compounds

Biological and Pharmacological Activities

Unknown, but of interest for research

Chemical Structure

Contains a fluorine atom attached to a phenyl ring, a propane chain with a 1,2-dione group, and an oxime functional group

Importance

Valuable tool for scientists and researchers in chemistry and medicine

Research Focus

Investigating its potential as a drug candidate or intermediate in the synthesis of other compounds

Safety

Unknown, but should be handled with care due to its potential reactivity and unknown biological effects

Stability

Unknown, but likely sensitive to heat, light, and moisture due to the presence of the oxime functional group

Check Digit Verification of cas no

The CAS Registry Mumber 395-07-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,9 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 395-07:
(5*3)+(4*9)+(3*5)+(2*0)+(1*7)=73
73 % 10 = 3
So 395-07-3 is a valid CAS Registry Number.

395-07-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2E)-1-(3-fluorophenyl)-2-hydroxyiminopropan-1-one

1.2 Other means of identification

Product number -
Other names 1-(3-fluoro-phenyl)-propane-1,2-dione-2-oxime

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:395-07-3 SDS

395-07-3Upstream product

395-07-3Downstream Products

395-07-3Relevant articles and documents

Nitrosocarbonyl-Henry and Denitration Cascade: Synthesis of α-Ketoamides and α-Keto Oximes

Reddy, Mallu Kesava,Mallik, Sumitava,Ramakrishna, Isai,Baidya, Mahiuddin

supporting information, p. 1694 - 1697 (2017/04/11)

An unprecedented Henry reaction of in situ generated nitrosocarbonyl intermediates and concomitant denitration cascade has been developed. The reaction is catalyzed by organic base at room temperature offering α-ketoamides, a demanding scaffold for drug discovery, in high yields. An alteration of substitution pattern also produced α-keto oximes, a high-value synthon. The protocol features operational simplicity and broad substrate scope.

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