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2-Hydroxymethyl-1-methyl-cyclohexanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 101869-72-1 Structure
  • Basic information

    1. Product Name: 2-Hydroxymethyl-1-methyl-cyclohexanol
    2. Synonyms: 2-Hydroxymethyl-1-methyl-cyclohexanol
    3. CAS NO:101869-72-1
    4. Molecular Formula:
    5. Molecular Weight: 144.214
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 101869-72-1.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: 2-Hydroxymethyl-1-methyl-cyclohexanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Hydroxymethyl-1-methyl-cyclohexanol(101869-72-1)
    11. EPA Substance Registry System: 2-Hydroxymethyl-1-methyl-cyclohexanol(101869-72-1)
  • 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: 101869-72-1(Hazardous Substances Data)

101869-72-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101869-72-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,8,6 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 101869-72:
(8*1)+(7*0)+(6*1)+(5*8)+(4*6)+(3*9)+(2*7)+(1*2)=121
121 % 10 = 1
So 101869-72-1 is a valid CAS Registry Number.

101869-72-1Relevant articles and documents

Hindered organoboron groups in organic chemistry. 21. The reactions of dimesitylboron stabilised carbanions with oxiranes

Peter, Andrew,Vaughan-Williams, Gina F.,Rosser, Richard M.

, p. 3007 - 3034 (1993)

Dimesitylboron stabilised carbanions react with oxiranes to give products that can be oxidised to 1,3-diols. The reactions are, in general, under steric rather than electronic control, and proceed smoothly for all but tetrasubstituted oxiranes. Some unusual stereoselective effects have been observed.

Regioselective mono-deprotection of di-ferf-butylsilylene acetal derived from 1,3-diol with ammonium fluoride

Ohtawa, Masaki,Tomoda, Hiroshi,Nagamitsu, Tohru

supporting information, p. 113 - 118 (2014/02/14)

Here we report a novel and efficient method for the regioselective mono-deprotection of di-terf-butylsilylene acetals derived from 1,3-diols consisting of primary and secondary alcohols. The ammonium fluoride-mediated reactions of pyripyropene A derivative, thymidine and uridine derivatives, methyl β-D-glucofuranoside, and pyranoside derivatives each gave the corresponding primary alcohol with high regioselectivity.

Direct catalytic asymmetric enolexo aldolizations

Pidathala, Chandrakala,Hoang, Linh,Vignola, Nicola,List, Benjamin

, p. 2785 - 2788 (2007/10/03)

32 years after the first, and still the only, catalytic asymmetric intramolecular aldol reaction was published in this journal, the proline-catalyzed Hajos-Parrish-Eder-Sauer-Wiechert reaction is extended for the first time to catalytic asymmetric enolexo

Rhodium-catalyzed reformatsky-type reaction

Kanai, Kazuo,Wakabayashi, Hitoshi,Honda, Toshio

, p. 2549 - 2551 (2007/10/03)

(equation presented) A novel Reformatsky-type reaction was developed using RhCl(PPh3)3 and diethylzinc. Inter- and intramolecular Reformatsky-type reactions were achieved efficiently under mild reaction conditions to give β-hydroxy esters.

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