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141195-10-0

(Z)-(2R,3S,7S)-7-Benzyloxy-2-(tert-butyl-dimethyl-silanyloxy)-oct-5-en-3-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 141195-10-0 Structure

  • Basic information

    1. Product Name: (Z)-(2R,3S,7S)-7-Benzyloxy-2-(tert-butyl-dimethyl-silanyloxy)-oct-5-en-3-ol
    2. Synonyms:
    3. CAS NO:141195-10-0
    4. Molecular Formula:
    5. Molecular Weight: 364.601
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 141195-10-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (Z)-(2R,3S,7S)-7-Benzyloxy-2-(tert-butyl-dimethyl-silanyloxy)-oct-5-en-3-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (Z)-(2R,3S,7S)-7-Benzyloxy-2-(tert-butyl-dimethyl-silanyloxy)-oct-5-en-3-ol(141195-10-0)
    11. EPA Substance Registry System: (Z)-(2R,3S,7S)-7-Benzyloxy-2-(tert-butyl-dimethyl-silanyloxy)-oct-5-en-3-ol(141195-10-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 141195-10-0(Hazardous Substances Data)

141195-10-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141195-10-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,1,9 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 141195-10:
(8*1)+(7*4)+(6*1)+(5*1)+(4*9)+(3*5)+(2*1)+(1*0)=100
100 % 10 = 0
So 141195-10-0 is a valid CAS Registry Number.

141195-10-0Downstream Products

141195-10-0Relevant articles and documents

Effective 1,5-asymmetric induction in tin(IV) chloride promoted reactions between aldehydes and (4-alkoxy-2-alkenyl)tributylstannanes

McNeill,Thomas

, p. 322 - 334 (2007/10/02)

Transmetallation of (S)-4-benzyloxy-2-pentenyl(tributyl)stannane (1) using tin(IV) chloride generates an allyltin trichloride which reacts in situ with aldehydes to give 1-substituted syn-(3Z)-5-benzyloxyhexenols with excellent stereoselectivity. With chiral aldehydes, the stereoselectivity of the reaction is dominated by the reagent, except for 2-alkoxyaldehydes which show matching and mismatching consistent with preferred Felkin-Anh diastereofacial selectivity.

1,5-Asymmetric induction in reactions of δ-alkoxyallylstannanes: Stereoselective reactions with chiral aldehydes

McNeill, Alan H.,Thomas, Eric J.

, p. 1369 - 1372 (2007/10/02)

Transmetallation of (4S,2E)-4-phenylmethoxypent-2-enyl(tributyl)stannane 1 using tin(IV)chloride generates a reagent which shows excellent 1 5-stereoselectivity in reactions with aldehydes: with chiral aldehydes, the stereochemical preference of the reage

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