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3-(5,5-dimethyl-1,3-dioxan-2-yl)but-2-en-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51575-59-8

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51575-59-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51575-59-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,5,7 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 51575-59:
(7*5)+(6*1)+(5*5)+(4*7)+(3*5)+(2*5)+(1*9)=128
128 % 10 = 8
So 51575-59-8 is a valid CAS Registry Number.

51575-59-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(5,5-Dimethyl-1,3-dioxan-2-yl)-2-buten-1-ol

1.2 Other means of identification

Product number -
Other names -

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:51575-59-8 SDS

51575-59-8Downstream Products

51575-59-8Relevant academic research and scientific papers

Synthesis of analogues of citranaxanthin and their activity in free radical scavenging

Zhang, Shaofeng,Liu, Yuan,Luo, Juan

, p. 257 - 260 (2016/07/06)

Citranaxanthin and its analogues were synthesised via a C5 unit elongation to substituted conjugated polyenes. Their free radical scavenging activity was measured by 1,1-diphenyl-2-picrylhydrazinyl spectrophotometric methods. Results indicated that the new compounds exhibited antioxidant activities. Three new analogues had stronger antioxidant activity than citranaxanthin.

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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