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1838-82-0

(±)-2-methylhex-1-en-3-ol is a chiral organic compound with the molecular formula C7H14O. It is a secondary alcohol and an alkene, featuring a methyl group at the 2nd carbon and a hydroxyl group at the 3rd carbon in a hexene chain. (±)-2-methylhex-1-en-3-ol is known for its distinct, fruity aroma and is commonly found in various fruits, such as apples and pears. Due to its chiral nature, it exists as a mixture of two enantiomers, which can be separated through chiral chromatography or other methods. (±)-2-methylhex-1-en-3-ol is also used as a flavoring agent in the food and beverage industry, contributing to the characteristic taste and smell of certain products.

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  • 1838-82-0 Structure

  • Basic information

    1. Product Name: (±)-2-methylhex-1-en-3-ol
    2. Synonyms: (±)-2-methylhex-1-en-3-ol
    3. CAS NO:1838-82-0
    4. Molecular Formula:
    5. Molecular Weight: 114.188
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1838-82-0.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: (±)-2-methylhex-1-en-3-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (±)-2-methylhex-1-en-3-ol(1838-82-0)
    11. EPA Substance Registry System: (±)-2-methylhex-1-en-3-ol(1838-82-0)

  • 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: 1838-82-0(Hazardous Substances Data)

1838-82-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1838-82-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,3 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1838-82:
(6*1)+(5*8)+(4*3)+(3*8)+(2*8)+(1*2)=100
100 % 10 = 0
So 1838-82-0 is a valid CAS Registry Number.

1838-82-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (±)-2-methylhex-1-en-3-ol

1.2 Other means of identification

Product number -
Other names (+/-)-2-methylhex-1-en-3-ol

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:1838-82-0 SDS

1838-82-0Relevant articles and documents

SYNTHESIS AND SOME REACTIONS OF ISOPROPENYLOXIRANE

Gevorkyan, A. A.,Kazaryan, P. I.,Avakyan, S. V.

, p. 372 - 378 (2007/10/02)

A convenient method for the synthesis of isopropenyloxirane by dehydrohalogenation of halohydrins obtained by isomerization of 1-halo-3-methyl-2,3-epoxybutanes was developed.The reactions of isopropenyloxirane with alcohols, water, secondary amines, hydrogen halides, dichlorocarbene, acetic acid anhydrides, and Grignard reagents were studied.

Studies on the Autoxidation of Branched-chain Olefins. I. Autoxidation of 2-Methylalk-1-enes and 2-Methylalk-2-enes

Bilas, W.,Hoebold, W.,Pritzkow, W.

, p. 125 - 141 (2007/10/02)

The products of the autoxidation of 2-methylpent-1-ene, 2-methylpent-2-ene, 2-methylhex-1-ene, 2-methylhex-2-ene, 2,4,4-trimethylpent-1-ene, and 2,4,4-trimethylpent-2-ene were analyzed by gas chromatography.The identification of the products corresponding to the individual peaks was possible by comparison with authentic substances or by preparative gaschromatographic separation and n.m.r.-spectroscopy of the isolated samples.In this way not only the epoxides and the products of the oxidative cleavage of the C=C double bond but also the allylic alcohols formed by LiAlH4-reduction of the oxidation mixtures could be identified and analyzed.From the results the compositions of the original oxidation mixtures were calculated.

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