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1-cyclohexyl-4-(tert-butyldimethylsilyloxy)-but-2-yne-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 462632-87-7 Structure
  • Basic information

    1. Product Name: 1-cyclohexyl-4-(tert-butyldimethylsilyloxy)-but-2-yne-1-ol
    2. Synonyms: 1-cyclohexyl-4-(tert-butyldimethylsilyloxy)-but-2-yne-1-ol
    3. CAS NO:462632-87-7
    4. Molecular Formula:
    5. Molecular Weight: 282.498
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 462632-87-7.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: 1-cyclohexyl-4-(tert-butyldimethylsilyloxy)-but-2-yne-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-cyclohexyl-4-(tert-butyldimethylsilyloxy)-but-2-yne-1-ol(462632-87-7)
    11. EPA Substance Registry System: 1-cyclohexyl-4-(tert-butyldimethylsilyloxy)-but-2-yne-1-ol(462632-87-7)
  • 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: 462632-87-7(Hazardous Substances Data)

462632-87-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 462632-87-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,2,6,3 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 462632-87:
(8*4)+(7*6)+(6*2)+(5*6)+(4*3)+(3*2)+(2*8)+(1*7)=157
157 % 10 = 7
So 462632-87-7 is a valid CAS Registry Number.

462632-87-7Relevant articles and documents

Stereoselective synthesis of (E)-β-tributylstannyl-α,β-unsaturated ketones: Construction of a key intermediate for the total synthesis of zoanthamine

Nielsen, Thomas E.,Tanner, David

, p. 6366 - 6371 (2002)

(E)-β-Trialkylstannyl-α,β-unsaturated ketones are readily available from secondary propargylic alcohols via a two-step sequence involving highly regio- and stereoselective Pd(0)-catalyzed hydrostannation followed by mild oxidation (TPAP). The methodology

α-fluoroallenoate synthesis via N-heterocyclic carbene-catalyzed fluorination reaction of alkynals

Wang, Xu,Wu, Zijun,Wang, Jian

supporting information, p. 576 - 579 (2016/02/18)

The first catalytic α-fluoroallenoate synthesis is described. With a suitable combination of N-heterocyclic carbene precatalyst, base, and fluorine reagent, the reaction proceeded smoothly to yield a wide range of α-fluoroallenoates with excellent chemose

Dynamic kinetic asymmetric allylic alkylations of allenes

Trost, Barry M.,Fandrick, Daniel R.,Dinh, Diana C.

, p. 14186 - 14187 (2007/10/03)

The dynamic kinetic asymmetric allylic alkylations of racemic allene acetates has been developed with the DACH-phenyl Trost ligand 2 to give general access to allenes with high enantiomeric excess (84-95%) for both malonate and amine nucleophiles. Further

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