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126917-44-0

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126917-44-0 Usage

Description

1-((R)-2-CHLORO-1-METHYLENE-PROPYL)-2,4-DIFLUORO-BENZENE is a complex and highly specific chiral organic compound characterized by its unique structure and potential applications across various industries. The presence of chlorine and fluorine atoms, along with the substituted benzene ring, suggests that this compound may possess special properties, making it a promising candidate for pharmaceutical or agrochemical uses.

Uses

Used in Pharmaceutical Industry:
1-((R)-2-CHLORO-1-METHYLENE-PROPYL)-2,4-DIFLUORO-BENZENE is used as an active pharmaceutical ingredient (API) for its potential therapeutic effects. 1-((R)-2-CHLORO-1-METHYLENE-PROPYL)-2,4-DIFLUORO-BENZENE's unique structure, including the (R)-designation and the presence of chlorine and fluorine atoms, may contribute to its efficacy in targeting specific biological pathways or receptors, leading to the development of novel drugs.
Used in Agrochemical Industry:
In the agrochemical sector, 1-((R)-2-CHLORO-1-METHYLENE-PROPYL)-2,4-DIFLUORO-BENZENE is used as a key intermediate in the synthesis of various agrochemical products. Its unique structure and properties may provide advantages in the development of new pesticides, herbicides, or other agricultural chemicals that can improve crop yield and protect against pests and diseases.
Used in Chemical Research:
1-((R)-2-CHLORO-1-METHYLENE-PROPYL)-2,4-DIFLUORO-BENZENE is also utilized as a research tool in the field of organic chemistry. Its chiral nature and the presence of multiple functional groups make it an interesting subject for studying reaction mechanisms, stereochemistry, and the development of new synthetic methods.
Used in Material Science:
1-((R)-2-CHLORO-1-METHYLENE-PROPYL)-2,4-DIFLUORO-BENZENE's aromatic properties and the presence of halogen atoms may make it suitable for use in the development of new materials with specific properties, such as improved thermal stability, chemical resistance, or electronic properties. It could be used as a building block or additive in the material science industry for creating innovative products with enhanced performance characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 126917-44-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,9,1 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 126917-44:
(8*1)+(7*2)+(6*6)+(5*9)+(4*1)+(3*7)+(2*4)+(1*4)=140
140 % 10 = 0
So 126917-44-0 is a valid CAS Registry Number.

126917-44-0SDS

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 (R)-3-chloro-2-(2,4-difluorophenyl)-1-butene

1.2 Other means of identification

Product number -
Other names 1-((R)-2-Chloro-1-methylene-propyl)-2,4-difluoro-benzene

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:126917-44-0 SDS

126917-44-0Relevant articles and documents

Concise Synthesis of Optically Active Oxirane Precursors for the Preparation of Triazole Antifungals Using the Friedel-Crafts Reaction of (S)-2-Tosyloxypropionyl Chloride

Konosu, Toshiyuki,Tajima, Yawara,Miyaoka, Takeo,Oida, Sadao

, p. 7545 - 7548 (2007/10/02)

Optically active epoxide (2R,3S)-4, a key intermediate for the preparation of triazole antifungal agents (4R,5R)-1 and (2R,3R)-2 (X = 2,4-F2), was synthesized.The Friedel-Crafts reaction between the (S)-lactic acid derivative (S)-10 and m-difluorobenzene gave the (R)-2-chloropropiophenone derivative (R)-11, which was converted into (2R,3R)-18 via Peterson olefination, stereoselective osmium(VIII) oxide oxidation, and mesylation.Treatment of (2R,3R)-18 with sodium triazolide gave (2R,3S)-4.Similarly, the 4-chlorophenyl analog (2R,3S)-4' was prepared.

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