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CAS

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10036-10-9

Bicyclo[3.3.1]nonan-3-ol, also known as 3-norbornanol, is a bicyclic organic compound with the chemical formula C7H12O. It is a white, waxy solid with a camphor-like odor.

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  • 10036-10-9 Structure

  • Basic information

    1. Product Name: bicyclo[3.3.1]nonan-3-ol
    2. Synonyms:
    3. CAS NO:10036-10-9
    4. Molecular Formula: C9H16O
    5. Molecular Weight: 140.2227
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 10036-10-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 229°C at 760 mmHg
    3. Flash Point: 93.3°C
    4. Appearance: N/A
    5. Density: 1.018g/cm3
    6. Vapor Pressure: 0.0137mmHg at 25°C
    7. Refractive Index: 1.509
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: bicyclo[3.3.1]nonan-3-ol(CAS DataBase Reference)
    11. NIST Chemistry Reference: bicyclo[3.3.1]nonan-3-ol(10036-10-9)
    12. EPA Substance Registry System: bicyclo[3.3.1]nonan-3-ol(10036-10-9)

  • 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: 10036-10-9(Hazardous Substances Data)

10036-10-9 Usage

Uses

Used in Pharmaceutical Industry:
Bicyclo[3.3.1]nonan-3-ol is used as a synthetic intermediate for the manufacture of pharmaceuticals, contributing to the development of various medications.
Used in Fragrance Industry:
It serves as a synthetic intermediate in the production of fragrances, enhancing the scent profiles of different perfumes and scented products.
Used in Flavoring Industry:
Bicyclo[3.3.1]nonan-3-ol is used as a synthetic intermediate in the creation of flavorings, adding unique taste elements to food and beverages.
Used in Solvent Applications:
It is utilized as a solvent in the production of cellulose esters, resins, and plasticizers, playing a crucial role in the formation of these materials.
Used in Organic Synthesis:
Bicyclo[3.3.1]nonan-3-ol has been studied for its potential use as a chiral building block in organic synthesis, indicating its importance in the development of complex organic compounds.
Safety Note:
Bicyclo[3.3.1]nonan-3-ol is considered to be relatively non-toxic, with low acute oral and dermal toxicity. However, exposure to high concentrations of its vapor can cause irritation to the respiratory system and central nervous system, necessitating proper handling and safety measures during its use.

Check Digit Verification of cas no

The CAS Registry Mumber 10036-10-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,3 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10036-10:
(7*1)+(6*0)+(5*0)+(4*3)+(3*6)+(2*1)+(1*0)=39
39 % 10 = 9
So 10036-10-9 is a valid CAS Registry Number.

10036-10-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name endo-Bicyclo[3.3.1]nonan-3-ol

1.2 Other means of identification

Product number -
Other names 2-phenoxyethyl 4-(2,3-dimethoxyphenyl)-7-(4-methoxyphenyl)-2-methyl-5-oxo-1,4,6,7,8-pentahydroquinoline-3-carboxylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10036-10-9 SDS

10036-10-9Relevant articles and documents

Bicyclononanes as Synthetic intermediates. IX.1) Photo-Irradiation of Bicycloalkan-3-one in Cyclohexane: A Selective Photo-Reduction with Predominance of endo-Hydrogenation

Momose, Takefumi,Muraoka, Osamu,Masuda, Kikuo

, p. 3730 - 3733 (2007/10/02)

Predominant formation of exo-alcohols in the photo-irradiation of bicyclononan-3-one and its analogs is described. Keywords --- bicyclononane system; selective photo-reduction; steric hindrance; intermolecular hydrogen abstraction; hydrogen-donor solvent.

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