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62285-84-1

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62285-84-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62285-84-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,8 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62285-84:
(7*6)+(6*2)+(5*2)+(4*8)+(3*5)+(2*8)+(1*4)=131
131 % 10 = 1
So 62285-84-1 is a valid CAS Registry Number.

62285-84-1SDS

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-(5,5-dimethyl-1,3-dioxan-2-yl)but-2-en-1-ol

1.2 Other means of identification

Product number -
Other names (E)-3-(5,5-dimethyl-1,3-dioxan-2-yl)-2-buten-1-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:62285-84-1 SDS

62285-84-1Downstream Products

62285-84-1Relevant articles and documents

Preparation of cyclic acetals of 3-formyl-2-butenyltriphenylphosphonium chloride

-

, (2008/06/13)

An improved process for preparing cyclic acetals of 3-formyl-2-butenyltriphenylphosphonium chloride by acetalization of 3-formyl-2-butenyl acetate with an aliphatic 1,3-diol, conversion of the resulting 4-acetoxy acetal into the corresponding 4-hydroxy acetal, Vilsmeier chlorination to give the corresponding 4-chloro acetal and subsequent reaction with triphenylphosphine entails carrying out the first 3 steps in an aliphatic or cycloaliphatic hydrocarbon or mixture of hydrocarbons with 6-8 carbons and the reaction with triphenylphosphine in an alkanol with 1-3 carbons and/or in aliphatic or cycloaliphatic hydrocarbon with 6-8 carbons or a corresponding mixture of hydrocarbons. The process is particularly advantageous when conversion of the 4-acetoxy acetal into the 4-hydroxy acetal is carried out with an aqueous alkali metal hydroxide solution in the presence of phase-transfer catalysts, and the first three, or all four, reaction stages are carried out in the same C6 -C8 -hydrocarbon.

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