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4-(3-hydroxybutyn-1-yl)-3,5,5-trimethylcyclohex-3-en-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

31162-45-5

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31162-45-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31162-45-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,1,6 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 31162-45:
(7*3)+(6*1)+(5*1)+(4*6)+(3*2)+(2*4)+(1*5)=75
75 % 10 = 5
So 31162-45-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H20O2/c1-9-7-11(15)8-13(3,4)12(9)6-5-10(2)14/h10-11,14-15H,7-8H2,1-4H3

31162-45-5SDS

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-(3-hydroxybut-1-ynyl)-3,5,5-trimethylcyclohex-3-en-1-ol

1.2 Other means of identification

Product number -
Other names megastigm-5-en-7-yne-3,9-diol

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:31162-45-5 SDS

31162-45-5Downstream Products

31162-45-5Relevant academic research and scientific papers

Precursors of Damascenone in Fruit Juices

Skouroumounis, George K.,Massy-Westropp, Ralph A.,Sefton, Mark A.,Williams, Patrick J.

, p. 3533 - 3536 (2007/10/02)

The acid-catalysed reactions of 6,7-megastigmadiene-3,5,9-triol and the β-D-glucosides of 5-megastigmen-7-yne-3,9-diol and 3-hydroxy-β-damascenone have been studied in relation to the formation of damascenone.The results show that hydrolysis of the allene triol could account for damascenone formation in the juices of grapes and other fruits.

Substituted alkynes useful as intermediates in the synthesis of carotenoids

-

, (2008/06/13)

Compounds of the formula STR1 wherein n is either 0 or 1; R1 and R2 is hydrogen and the other is hydrogen, hydroxy, oxo group, a protected hydroxy or protected oxo group; R3 is hydroxy oxo group, =CH--CH2 --OH, =CH--CHO or one of the foregoing groups where the hydroxy or oxo functions are protected; R4 is --CO--OR6, --CO--R6, --CO--NR6 R7, --CO--Cl or --SO2 --R6 ; R6 is saturated or aromatic hydrocarbon; and R7 is saturated or aromatic hydrocarbon or hydrogen, are converted by cleavage of R4 OH into corresponding cycloalkenes and protecting groups, if present, are hydrolyzed. The compounds obtained are valuable intermediates in carotenoid syntheses.

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