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933779-95-4

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  • (5Z,7E)-(1R,2R,3R)-1,3-bis(tert-butyldimethylsilyloxy)-2-(3-tert-butyldimethylsilyloxypropoxy)-25-triethylsilyloxy-9,10-secocholesta-5,7,10(19)-triene

    Cas No: 933779-95-4

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933779-95-4 Usage

Description

(5Z,7E)-(1R,2R,3R)-1,3-bis(tert-butyldimethylsilyloxy)-2-(3-tert-butyldimethylsilyloxypropoxy)-25-triethylsilyloxy-9,10-secocholesta-5,7,10(19)-triene is a complex organic compound with a unique molecular structure. It is a derivative of 9,10-secocholesta-5,7,10(19)-triene, featuring various substituents such as tert-butyldimethylsilyloxy and triethylsilyloxy groups. (5Z,7E)-(1R,2R,3R)-1,3-bis(tert-butyldimethylsilyloxy)-2-(3-tert-butyldimethylsilyloxypropoxy)-25-triethylsilyloxy-9,10-secocholesta-5,7,10(19)-triene is likely used in organic synthesis and chemical research, serving as a precursor or intermediate in the production of other compounds or materials. The presence of multiple functional groups suggests that it may have specific reactivity and utility in various chemical reactions and processes.

Uses

Used in Organic Synthesis:
(5Z,7E)-(1R,2R,3R)-1,3-bis(tert-butyldimethylsilyloxy)-2-(3-tert-butyldimethylsilyloxypropoxy)-25-triethylsilyloxy-9,10-secocholesta-5,7,10(19)-triene is used as a precursor or intermediate in the synthesis of other complex organic compounds. Its unique molecular structure and functional groups make it a valuable building block for the development of new molecules with specific properties and applications.
Used in Chemical Research:
(5Z,7E)-(1R,2R,3R)-1,3-bis(tert-butyldimethylsilyloxy)-2-(3-tert-butyldimethylsilyloxypropoxy)-25-triethylsilyloxy-9,10-secocholesta-5,7,10(19)-triene is also used in chemical research to study its reactivity and properties. The presence of multiple functional groups allows researchers to explore various chemical reactions and processes, potentially leading to the discovery of new synthetic routes or applications for this compound.
Used in Pharmaceutical Industry:
(5Z,7E)-(1R,2R,3R)-1,3-bis(tert-butyldimethylsilyloxy)-2-(3-tert-butyldimethylsilyloxypropoxy)-25-triethylsilyloxy-9,10-secocholesta-5,7,10(19)-triene may have potential applications in the pharmaceutical industry as a starting material for the synthesis of bioactive compounds or as a modifier to improve the properties of existing drugs.
Used in Material Science:
(5Z,7E)-(1R,2R,3R)-1,3-bis(tert-butyldimethylsilyloxy)-2-(3-tert-butyldimethylsilyloxypropoxy)-25-triethylsilyloxy-9,10-secocholesta-5,7,10(19)-triene's unique structure and functional groups may also find applications in material science, where it could be used to develop new materials with specific properties, such as improved stability, reactivity, or selectivity in various chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 933779-95-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,3,7,7 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 933779-95:
(8*9)+(7*3)+(6*3)+(5*7)+(4*7)+(3*9)+(2*9)+(1*5)=224
224 % 10 = 4
So 933779-95-4 is a valid CAS Registry Number.

933779-95-4Downstream Products

933779-95-4Relevant articles and documents

Two convergent approaches to the synthesis of 1,25-dihydroxy 2-(3-hydroxypropoxy)vitamin D3 (ED-71) by the lythgoe and thf trost coupling reactions

Maeyama, Junji,Hiyamizu, Hiroko,Takahashi, Keisuke,Ishihara, Jun,Hatakeyama, Susumi,Kubodera, Noboru

, p. 295 - 307 (2008/04/18)

Two convergent syntheses of 1,25-dihydroxy-2-(3-hydroxypropoxy)vitamin D3 (ED-71) by the Lythgoe coupling reaction between the A-ring phosphine oxide and the C/D-ring ketone and the Trost coupling reaction between the A-ring ene-yne and the C/D-ring bromomethylene are described.

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