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132054-64-9

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  • (1S,5R,Z)-5-(tert-butyldiMethylsilyloxy)-3-((E)-2-((1R,3aS,7aR)-1-((R)-6-hydroxy-6-Methylheptan-2-yl)-7a-Methyldihydro-1H-inden-4(2H,5H,6H,7H,7aH)-ylidene)ethylidene)-2-Methylenecyclohexanol

    Cas No: 132054-64-9

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132054-64-9 Usage

Description

(1S,5R,Z)-5-(tert-butyldiMethylsilyloxy)-3-((E)-2-((1R,3aS,7aR)-1-((R)-6-hydroxy-6-Methylheptan-2-yl)-7a-Methyldihydro-1H-inden-4(2H,5H,6H,7H,7aH)-ylidene)ethylidene)-2-Methylenecyclohexanol is a complex organic compound with a cyclohexanol core and multiple side chains and functional groups. It features a tert-butyldimethylsilyloxy group, hydroxyl groups, and a conjugated diene system. Additionally, it contains a dihydroindenylidene moiety, making it a highly specific and specialized compound.

Uses

Used in Organic Synthesis:
(1S,5R,Z)-5-(tert-butyldiMethylsilyloxy)-3-((E)-2-((1R,3aS,7aR)-1-((R)-6-hydroxy-6-Methylheptan-2-yl)-7a-Methyldihydro-1H-inden-4(2H,5H,6H,7H,7aH)-ylidene)ethylidene)-2-Methylenecyclohexanol is used as a building block in organic synthesis for the creation of more complex molecules and structures.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, this compound serves as a potential candidate for the development of new drugs and pharmaceuticals due to its unique structure and functional groups.
Used in Chemical Research:
(1S,5R,Z)-5-(tert-butyldiMethylsilyloxy)-3-((E)-2-((1R,3aS,7aR)-1-((R)-6-hydroxy-6-Methylheptan-2-yl)-7a-Methyldihydro-1H-inden-4(2H,5H,6H,7H,7aH)-ylidene)ethylidene)-2-Methylenecyclohexanol is utilized in chemical research to study its properties, reactivity, and potential applications in various chemical processes.
Used in Specialty Chemicals Industry:
(1S,5R,Z)-5-(tert-butyldiMethylsilyloxy)-3-((E)-2-((1R,3aS,7aR)-1-((R)-6-hydroxy-6-Methylheptan-2-yl)-7a-Methyldihydro-1H-inden-4(2H,5H,6H,7H,7aH)-ylidene)ethylidene)-2-Methylenecyclohexanol is also used in the specialty chemicals industry for the development of high-value products with specific applications, such as advanced materials, coatings, or catalysts.

Check Digit Verification of cas no

The CAS Registry Mumber 132054-64-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,0,5 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 132054-64:
(8*1)+(7*3)+(6*2)+(5*0)+(4*5)+(3*4)+(2*6)+(1*4)=89
89 % 10 = 9
So 132054-64-9 is a valid CAS Registry Number.

132054-64-9SDS

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 (1S,3E,5R)-3-[(2Z)-2-[(1R,3aS,7aR)-1-[(2R)-6-hydroxy-6-methylheptan-2-yl]-3a,7a-dimethyl-1,2,3,5,6,7-hexahydroinden-4-ylidene]ethylidene]-5-[tert-butyl(dimethyl)silyl]oxy-2-methylidenecyclohexan-1-ol

1.2 Other means of identification

Product number -
Other names (1S,5R,Z)-5-(tert-butyldimethylsilyloxy)-3-((E)-2-((1R,3aS,7aR)-1-((R)-6-hydroxy-6-methylheptan-2-yl)-7a-methyldihydro-1H-inden-4(2H,5H,6H,7H,7aH)-ylidene)ethylidene)-2-Methylenecyclohexanol

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:132054-64-9 SDS

132054-64-9Relevant articles and documents

1α,25-Dihydroxyvitamin D3-3β-bromoacetate, a potential cancer therapeutic agent: Synthesis and molecular mechanism of action

Ray, Rahul,Lambert, James R.

, p. 2537 - 2540 (2011/06/11)

Synthesis of 1α,25-dihydroxyvitamin D3-3β- bromoacetate (1,25(OH)2D3-3-BE), a potential anti-cancer agent is presented. We also report that mechanism of action of 1,25(OH) 2D3-3-BE may involve reducti

A direct, regio- and stereoselective 1α-hydroxylation of (5E)-calciferol derivatives

Andrews,Barton,Cheng,et al.

, p. 1635 - 1637 (2007/10/02)

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