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6478-04-2

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6478-04-2 Usage

Physical state

Colorless to light yellow liquid

Odor

Pungent

Usage

Reactive intermediate in the production of various chemical compounds

Applications

Synthesis of pharmaceuticals, agrochemicals, and other organic compounds

Role in organic chemistry

Reagent in organic chemistry reactions, preparation of thiol derivatives

Safety precautions

Corrosive and harmful if not properly managed, handle with care

Check Digit Verification of cas no

The CAS Registry Mumber 6478-04-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,7 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6478-04:
(6*6)+(5*4)+(4*7)+(3*8)+(2*0)+(1*4)=112
112 % 10 = 2
So 6478-04-2 is a valid CAS Registry Number.
InChI:InChI=1/C3H7ClOS/c4-1-3(5)2-6/h3,5-6H,1-2H2

6478-04-2SDS

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 1-chloro-3-sulfanylpropan-2-ol

1.2 Other means of identification

Product number -
Other names 1-chloro-3-mercapto-propan-2-ol

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:6478-04-2 SDS

6478-04-2Relevant articles and documents

Sulfur-containing epoxy compound and its manufacturing method

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Paragraph 0072; 0073, (2017/07/04)

The invention provides a sulfur-containing epoxy component which is stable and does not generate white turbidness when is stored at room temperature, and a method thereof. To solve the problem, the sulfur-containing epoxy compound is manufactured by using hydrogen sulfide or polythiol compound and epichlorohydrin which has a turbidity value below 1.0ppm while manufacturing 30 mass% methanol solution and the manufacturing method are used.

Method of Producing Thioepoxy Compound for Optical Material and Polymerizable Composition for Thioepoxy based Optical Material Comprising the Compound

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Paragraph 0063; 0064, (2017/07/04)

The present invention relates to a thioepoxy compound from which a high-quality optical material having a good and clear color and causing no whitening can be obtained, and a polymerizable composition for a thioepoxy-based optical material comprising the same. The present invention provides a method for preparing a thioepoxy compound for an optical material, which uses an epichlorohydrin compound as a starting material, wherein the epichlorohydrin compound has a total content of specific impurities, including acrolein, allyl chloride, 1,2-dichloropropane and 2,3-dichloropropene, of 1 wt% or less. According to the present invention, it is possible to obtain a thioepoxy compound causing less coloration by adjusting the content of specific impurities in the epichlorohydrin compound. In addition, the resultant thioepoxy compound can be used to obtain a high-quality transparent thioepoxy-based optical material having a good color and causing no whitening. The thioepoxy-based optical material according to the present invention is useful for corrective lenses, sunglass lenses, fashion lenses, metachrosis lenses, camera lenses, and lenses for optical devices.COPYRIGHT KIPO 2016

NOVEL METHOD FOR PREPARING POLYTHIOL COMPOUND AND POLYMERIC COMPOSITION FOR OPTICAL MATERIAL COMPRISING SAME

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Paragraph 0041; 0042, (2015/06/03)

The present invention relates to novel methods for preparing a polythiol compound for use in an optical material and polymerizable compositions including a polythiol compound prepared by the methods. According to the methods, a polythiol compound with uniform color, high purity and high quality can be prepared at reduced cost. The polymerizable compositions can be used to manufacture clear, transparent optical lenses with good heat resistance and excellent optical properties.

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