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15606-89-0

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15606-89-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15606-89-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,6,0 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15606-89:
(7*1)+(6*5)+(5*6)+(4*0)+(3*6)+(2*8)+(1*9)=110
110 % 10 = 0
So 15606-89-0 is a valid CAS Registry Number.

15606-89-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyloxathiolane 2,2-dioxide

1.2 Other means of identification

Product number -
Other names 4-methyl-[1,2]oxathiolane-2,2-dioxide

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:15606-89-0 SDS

15606-89-0Upstream product

15606-89-0Downstream Products

15606-89-0Relevant articles and documents

-

Smith et al.

, p. 748 (1953)

-

Method for preparing 2-methyl-1,3-propane sultone

-

Paragraph 0036; 0040, (2018/07/30)

The invention discloses a method for preparing 2-methyl-1,3-propane sultone. The method comprises the following steps: (1) mixing 2-methyl-1,3-propylene glycol with a chlorinating agent, performing achlorination reaction at a certain temperature, and after the reaction is completed, concentrating and removing the solution so as to obtain 2-methyl-1,3-propylene dichloride; (2) mixing the obtained2-methyl-1,3-propylene dichloride with a sulfonating agent and a solvent, increasing the temperature to implement a sulfonation reaction, and stirring till the reaction is completed so as to obtain 2-methyl 3-sodium chloropropyl sulfonate; (3) putting the obtained 2-methyl 3-sodium chloropropyl sulfonate into water, adding a strong acid to adjust the pH value to be 1-3, performing acidification treatment, removing inorganic salts through concentration and filtration, and further concentrating till dryness so as to obtain 2-methyl-3-chlorine propanesulfonate; (4) heating the obtained 2-methyl-3-chlorine propanesulfonate under a vacuum condition, performing dehydrochlorination, and performing an internal esterification reaction, so as to obtain 2-methyl-1,3-propane sultone. The method has the advantages of being small in raw material toxicity, cheap in raw material, easy in raw material obtaining, easy in on-scale production, high in product purity, high in product yield, and the like.

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