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(+/-)-(1-hydroxy-octyl)-cyclohexane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 108693-51-2 Structure
  • Basic information

    1. Product Name: (+/-)-(1-hydroxy-octyl)-cyclohexane
    2. Synonyms: (+/-)-(1-hydroxy-octyl)-cyclohexane
    3. CAS NO:108693-51-2
    4. Molecular Formula:
    5. Molecular Weight: 212.376
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 108693-51-2.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-hydroxy-octyl)-cyclohexane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (+/-)-(1-hydroxy-octyl)-cyclohexane(108693-51-2)
    11. EPA Substance Registry System: (+/-)-(1-hydroxy-octyl)-cyclohexane(108693-51-2)
  • 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: 108693-51-2(Hazardous Substances Data)

108693-51-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108693-51-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,6,9 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 108693-51:
(8*1)+(7*0)+(6*8)+(5*6)+(4*9)+(3*3)+(2*5)+(1*1)=142
142 % 10 = 2
So 108693-51-2 is a valid CAS Registry Number.

108693-51-2Downstream Products

108693-51-2Relevant articles and documents

A new type of complex reagent, R4Pb / TiCl4

Yamamoto, Yoshinori,Yamada, Jun-Ichi,Asano, Tetsuya

, p. 5587 - 5596 (2007/10/02)

Tetraalkllleads (R4Pb) reacted quite smoothly with aldehydes R'CHO in the presence of TiCl4 to produce the corresponding alcohols (RCHOHR′) in high to good yields. The reagent system, R4Pb/ TiCl4, exhibited high chemoselectivity; only aldehydes underwent the alkylation in the presence of ketones. Further, the new reagent exhibited high 1,2- and 1,3-asymmetric induction. The transfer order of alkyl groups in the reaction of aldehydes with mixed tetraalkylleads/TiCl4 was determined; Me>Et.i-Pr?n-Bu.

Geminal prostaglandin analogs

-

, (2008/06/13)

Geminal prostaglandins (P.G.'s) are synthesized which are represented by the general formula: STR1 where A is a 4 or 5 carbon atom ring-completing group (CH2)1+m --X--(CH2)z where m = 0, 1 or 2, Z = 0 or 1, 02 --CH2 --, --CH2 --CHOH--, STR2 and, when m = 0 and z = 1, is also --CH=CH-- or STR3 Y is divalent straight chain alkylene of 4 to 8 carbon atoms or r is alkyl of 4 to 7 carbon atoms; Q is --CO2 H or --CH2 OH provided that it is not --CH2 OH when X = STR4 or Y--Q taken together may be heptyl or allyl.

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