Cas 1092075-00-7,(Z)-2,5-bis(tert-butyldimethylsilyl)-1-cyclohexylpent-2-en-4-yn-1-ol

1092075-00-7

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Basic information

Product Name: (Z)-2,5-bis(tert-butyldimethylsilyl)-1-cyclohexylpent-2-en-4-yn-1-ol
Synonyms: (Z)-2,5-bis(tert-butyldimethylsilyl)-1-cyclohexylpent-2-en-4-yn-1-ol
CAS NO:1092075-00-7
Molecular Formula:
Molecular Weight: 392.773
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (Z)-2,5-bis(tert-butyldimethylsilyl)-1-cyclohexylpent-2-en-4-yn-1-ol(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-2,5-bis(tert-butyldimethylsilyl)-1-cyclohexylpent-2-en-4-yn-1-ol(1092075-00-7)
EPA Substance Registry System: (Z)-2,5-bis(tert-butyldimethylsilyl)-1-cyclohexylpent-2-en-4-yn-1-ol(1092075-00-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1092075-00-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1092075-00-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,2,0,7 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1092075-00:
(9*1)+(8*0)+(7*9)+(6*2)+(5*0)+(4*7)+(3*5)+(2*0)+(1*0)=127
127 % 10 = 7
So 1092075-00-7 is a valid CAS Registry Number.

1092075-00-7Upstream product

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1092075-00-7Relevant academic research and scientific papers

Dialkyltitanium-mediated titanation of conjugated 1,3-butadiynes and its coupling reactions with aldehydes: a facile synthesis of stereodefined enynes and trans-enynols

Chen, Jingjin,Liu, Yuanhong

supporting information; experimental part, p. 6655 - 6658 (2009/04/07)

A highly efficient and convenient method for the selective titanation of 1,3-butadiynes using Ti(OiPr)4/nBuLi reagent has been developed. The method provided a facile synthesis of enynes and trans-enynols in a well-stereod

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