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139013-68-6

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139013-68-6 Usage

Description

(S)-4-Chloro-1,3-butanediol, with the chemical formula C4H9ClO2, is a derivative of butanediol characterized by its specific (S)-enantiomer arrangement. (S)-4-Chloro-1,3-butanediol is known for its versatile applications in various industries due to its unique structural properties.

Uses

Used in Pharmaceutical Industry:
(S)-4-Chloro-1,3-butanediol is used as a building block for the synthesis of various pharmaceuticals, contributing to the development of new drugs and improving existing ones. Its unique structure allows for the creation of chiral molecules, which are essential in the pharmaceutical field.
Used in Agrochemical Industry:
In the agrochemical sector, (S)-4-Chloro-1,3-butanediol serves as a key intermediate in the production of agrochemicals, such as pesticides and herbicides. Its specific arrangement of atoms enables the synthesis of effective and targeted agrochemicals.
Used in Specialty Chemicals Production:
(S)-4-Chloro-1,3-butanediol is utilized as an intermediate in the synthesis of specialty chemicals, which are used in various applications, including coatings, adhesives, and sealants. Its unique properties make it a valuable component in these industries.
Used as a Solvent:
(S)-4-Chloro-1,3-butanediol is employed as a solvent in various chemical processes due to its ability to dissolve a wide range of substances. Its solubility properties make it a useful component in the production of various materials.
Used in Polymer Production:
(S)-4-Chloro-1,3-butanediol is also used as an intermediate in the production of polymers, which are essential in the manufacturing of plastics, fibers, and other materials. The specific arrangement of atoms in (S)-4-Chloro-1,3-butanediol allows for the creation of polymers with unique properties.
Used in Organic Chemistry Research:
(S)-4-Chloro-1,3-butanediol has potential applications in the field of organic chemistry, particularly in the development of new reactions and processes. Its unique structure provides opportunities for researchers to explore novel chemical pathways and syntheses.

Check Digit Verification of cas no

The CAS Registry Mumber 139013-68-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,0,1 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 139013-68:
(8*1)+(7*3)+(6*9)+(5*0)+(4*1)+(3*3)+(2*6)+(1*8)=116
116 % 10 = 6
So 139013-68-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H9ClO2/c5-3-4(7)1-2-6/h4,6-7H,1-3H2/t4-/m0/s1

139013-68-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S)-4-Chloro-1,3-butanediol

1.2 Other means of identification

Product number -
Other names 4-Chloro-1,2-diaminobenzene

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:139013-68-6 SDS

139013-68-6Downstream Products

139013-68-6Relevant articles and documents

PROCESS FOR THE EFFICIENT PREPARATION OF 3-HYDROXYTETRAHYDROFURAN

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Paragraph 89-90, (2008/12/07)

Disclosed is a process for the efficient preparation of 3-hydroxytetrahydrofuran. In particular, the present invention provides a process for the preparation of 3-hydroxytetrahydrofuran by performing cyclization of 4-halo-1,3-butanediol either neat or in an organic solvent by heating to 75°C to 18O°C. In the present invention, acidic solution is not used in the cyclization and, thus, the reaction environment is improved. Further, the cyclization product 3-hydroxytetrahydrofuran is purified by a simple process. In addition, according to the present invention, chirality of the starting material is substantially maintained. Consequently, chiral 3-hydroxytetrahydrofuran with a high optical purity of 99.0% ee or better can be prepared economically, in high yield.

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