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CAS

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123826-96-0

(1α,2β,3β,5α)-3-<2<<(1,1-dimethylethyl)diphenylsilyl>oxy>ethyl>-6-methylbicyclo<3.1.0>hexan-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 123826-96-0 Structure

  • Basic information

    1. Product Name: (1α,2β,3β,5α)-3-<2<<(1,1-dimethylethyl)diphenylsilyl>oxy>ethyl>-6-methylbicyclo<3.1.0>hexan-2-ol
    2. Synonyms:
    3. CAS NO:123826-96-0
    4. Molecular Formula:
    5. Molecular Weight: 394.629
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 123826-96-0.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: (1α,2β,3β,5α)-3-<2<<(1,1-dimethylethyl)diphenylsilyl>oxy>ethyl>-6-methylbicyclo<3.1.0>hexan-2-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1α,2β,3β,5α)-3-<2<<(1,1-dimethylethyl)diphenylsilyl>oxy>ethyl>-6-methylbicyclo<3.1.0>hexan-2-ol(123826-96-0)
    11. EPA Substance Registry System: (1α,2β,3β,5α)-3-<2<<(1,1-dimethylethyl)diphenylsilyl>oxy>ethyl>-6-methylbicyclo<3.1.0>hexan-2-ol(123826-96-0)

  • 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: 123826-96-0(Hazardous Substances Data)

123826-96-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123826-96-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,8,2 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 123826-96:
(8*1)+(7*2)+(6*3)+(5*8)+(4*2)+(3*6)+(2*9)+(1*6)=130
130 % 10 = 0
So 123826-96-0 is a valid CAS Registry Number.

123826-96-0Relevant articles and documents

Use of Radical Ring-Opening for Introduction of Alkyl and Substituted Alkyl Groups with Stereochemical Control: A Synthetic Application of Cyclopropylcarbinyl Radicals

Clive, Derrick L. J.,Daigneault, Sylvain

, p. 3801 - 3814 (1991)

Cyclopropylcarbinols 2a and 2b (see Scheme I), which are accessible by a number of routes, can be converted into the corresponding radicals 3a and 3b, respectively.These radicals undergo peripheral ring-opening of the cyclopropyl substructure to afford su

Synthetic Applications of Radical Ring-Opening: Use of Cyclopropylmethyl Radicals

Clive, Derrick L. J.,Daigneault, Sylvain

, p. 332 - 335 (2007/10/02)

Cycloropanation of cyclic allylic alcohols followed by radical deoxygenation leads, by peripheral ring-opening of the cyclopropylmethyl system, to alkyl-substituted cycloalkenes (Scheme 1); the alkyl group can itself be substituted (during the cyclopropan

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