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136374-71-5

(3-Hydroxymethyl-5-methoxymethyl-cyclohexyl)-methanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 136374-71-5 Structure

  • Basic information

    1. Product Name: (3-Hydroxymethyl-5-methoxymethyl-cyclohexyl)-methanol
    2. Synonyms:
    3. CAS NO:136374-71-5
    4. Molecular Formula:
    5. Molecular Weight: 188.267
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 136374-71-5.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: (3-Hydroxymethyl-5-methoxymethyl-cyclohexyl)-methanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3-Hydroxymethyl-5-methoxymethyl-cyclohexyl)-methanol(136374-71-5)
    11. EPA Substance Registry System: (3-Hydroxymethyl-5-methoxymethyl-cyclohexyl)-methanol(136374-71-5)

  • 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: 136374-71-5(Hazardous Substances Data)

136374-71-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136374-71-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,3,7 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 136374-71:
(8*1)+(7*3)+(6*6)+(5*3)+(4*7)+(3*4)+(2*7)+(1*1)=135
135 % 10 = 5
So 136374-71-5 is a valid CAS Registry Number.

136374-71-5Downstream Products

136374-71-5Relevant articles and documents

A novel method of synthesis of 1-azaadamantane from 1-boraadamantane

Bubnov, Yu. N.,Gursky, M. E.,Pershin, D. G.

, p. 1 - 8 (1991)

A novel and convenient method for the synthesis of 1-azaadamantane (I) from the 1-boraadamantane-tetrahydrofuran complex (XIII) is described.This is based on an intramolecular reaction of organic azides with organoboron compounds.Treatment of the boron cage compound XIII with iodine and an excess of sodium azide followed by oxidation (H2O2, OH-) affords 7α-hydroxymethyl-3-azabicyclononane (VII), cyclization of which leads to I in 40percent overall yield.Some new boron cage compounds were also isolated, diazidoborane (XIV) being of particular interest.

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