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628-09-1

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628-09-1 Usage

Description

3-Chloropropyl acetate, also known as 1-chloro-3-methoxy-2-propanol acetate, is a clear colorless liquid that serves as a crucial intermediate in various chemical reactions. It is primarily used in organic synthesis and has significant applications in the pharmaceutical, agrochemical, and dyestuff industries. Upon reaction with a strong base, 3-chloropropyl acetate yields trimethylene oxide, which further expands its utility in chemical processes.

Uses

Used in Organic Synthesis:
3-Chloropropyl acetate is used as a key intermediate for organic synthesis due to its reactive nature and ability to yield trimethylene oxide upon reaction with strong bases. This makes it a valuable component in the creation of various chemical compounds and materials.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-chloropropyl acetate is utilized as a building block for the synthesis of various drugs and medicinal compounds. Its versatility in chemical reactions allows for the development of new pharmaceutical agents with potential therapeutic applications.
Used in Agrochemicals:
3-Chloropropyl acetate is employed as a raw material in the production of agrochemicals, such as pesticides and herbicides. Its role in these applications is to provide a stable and effective platform for the development of compounds that can protect crops and enhance agricultural productivity.
Used in Dyestuff Industry:
In the dyestuff industry, 3-chloropropyl acetate is used as an essential component in the synthesis of various dyes and pigments. Its chemical properties make it suitable for creating a wide range of colorants used in textiles, plastics, and other materials.

Synthesis Reference(s)

Organic Syntheses, Coll. Vol. 3, p. 203, 1955The Journal of Organic Chemistry, 48, p. 751, 1983 DOI: 10.1021/jo00153a031

Check Digit Verification of cas no

The CAS Registry Mumber 628-09-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 628-09:
(5*6)+(4*2)+(3*8)+(2*0)+(1*9)=71
71 % 10 = 1
So 628-09-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H9ClO2/c1-5(7)8-4-2-3-6/h2-4H2,1H3

628-09-1 Well-known Company Product Price

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  • Alfa Aesar

  • (B25013)  3-Chloropropyl acetate, 98%   

  • 628-09-1

  • 25g

  • 366.0CNY

  • Detail
  • Alfa Aesar

  • (B25013)  3-Chloropropyl acetate, 98%   

  • 628-09-1

  • 100g

  • 659.0CNY

  • Detail
  • Alfa Aesar

  • (B25013)  3-Chloropropyl acetate, 98%   

  • 628-09-1

  • 500g

  • 2597.0CNY

  • Detail

628-09-1SDS

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 3-Chloropropyl acetate

1.2 Other means of identification

Product number -
Other names 3-Chlorprop-1-ylacetat

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:628-09-1 SDS

628-09-1Relevant articles and documents

Method for protection from AZT side effects and toxicity

-

, (2008/06/13)

S-ω(ω-aminoalkylamino)alkyl dihydrogen phosphorothioates or pharmaceutically acceptable derivatives thereof are useful in protecting a patient undergoing AZT treatment for AIDS and AIDS-related complex from the harmful side effects or reactions and toxici

EFFECT OF NATURE OF LIGANDS ON CATALYTIC DECOMPOSITION OF 2-METHYLTETRAHYDRO-2-FURYL HYDROPEROXIDE BY IRON SALTS

Glukhovtsev, V. G.,Il'in, Yu. V.,Nikishin, G. I.

, p. 1479 - 1482 (2007/10/02)

-

NEW SYSTEM FOR DETERMINING THE ACTIVITY OF CARBON-HYDROGEN BONDS IN REACTIONS WITH ALKOXYL RADICALS

Zorin, V. V.,Zlotskii, S. S.,Glukhovtsev, V. G.,Il'in, Yu. V.,Nikishin, G. I.,Rakhmankulov, D. L.

, p. 231 - 234 (2007/10/02)

In a medium containing a donor of hydrogen atoms and carbon tetrachloride 2-methyltetrahydrofuran-2-oxyl radicals are consumed in parallel reactions leading to acetopropyl alcohol and 3-chloropropyl acetate.It was shown that the reactivity of the hydrogen donor with respect to 2-methyltetrahydrofuran-2-oxyl radicals can be estimated quantitatively from determination of the paths for the consumption of the radicals.The ratios of the rate constants for the abstraction of a hydrogen atom from organic compounds by 2-methyltetrahydrofuran-2-oxyl radicals to the rate constants for its rearrangement to 3-acetoxypropyl radical were determined.

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