Welcome to LookChem.com Sign In|Join Free

CAS

  • or
octane-3,6-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24434-09-1 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 24434-09-1 Structure
  • Basic information

    1. Product Name: octane-3,6-diol
    2. Synonyms: 3,6-octanediol; Octane-3,6-diol
    3. CAS NO:24434-09-1
    4. Molecular Formula: C8H18O2
    5. Molecular Weight: 146.2273
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 24434-09-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 240.8°C at 760 mmHg
    3. Flash Point: 124.5°C
    4. Appearance: N/A
    5. Density: 0.935g/cm3
    6. Vapor Pressure: 0.00645mmHg at 25°C
    7. Refractive Index: 1.45
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: octane-3,6-diol(CAS DataBase Reference)
    11. NIST Chemistry Reference: octane-3,6-diol(24434-09-1)
    12. EPA Substance Registry System: octane-3,6-diol(24434-09-1)
  • 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: 24434-09-1(Hazardous Substances Data)

24434-09-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24434-09-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,3 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24434-09:
(7*2)+(6*4)+(5*4)+(4*3)+(3*4)+(2*0)+(1*9)=91
91 % 10 = 1
So 24434-09-1 is a valid CAS Registry Number.

24434-09-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name octane-3,6-diol

1.2 Other means of identification

Product number -
Other names 3,6-Octanediol

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:24434-09-1 SDS

24434-09-1Downstream Products

24434-09-1Relevant articles and documents

Biocatalytic synthesis of non-vicinal aliphatic diols

Ebrecht, Ana C.,Aschenbrenner, Jasmin C.,Smit, Martha S.,Opperman, Diederik J.

supporting information, p. 439 - 445 (2021/01/29)

Biocatalysts are receiving increased attention in the field of selective oxyfunctionalization of C-H bonds, with cytochrome P450 monooxygenases (CYP450s), and the related peroxygenases, leading the field. Here we report on the substrate promiscuity of CYP505A30, previously characterized as a fatty acid hydroxylase. In addition to its regioselective oxyfunctionalization of saturated fatty acids (ω-1-ω-3 hydroxylation), primary fatty alcohols are also accepted with similar regioselectivities. Moreover, alkanes such as n-octane and n-decane are also readily accepted, allowing for the production of non-vicinal diols through sequential oxygenation. This journal is

Extracts of Isochrysis sp.

-

, (2010/04/25)

The present invention relates to extracts of Isochrysis sp., preferably Tahitian Isochrysis, its cosmetic, dermatological and/or therapeutic uses and compositions and cosmetic, dermatological or therapeutic products comprising such an extract of Isochrysis sp., preferably Tahitian Isochrysis.

Extracts of isochrysis sp.

-

, (2010/04/25)

The present invention relates to extracts of Isochrysis sp., preferably Tahitian Isochrysis, its cosmetic, dermatological and/or therapeutic uses and compositions and cosmetic, dermatological or therapeutic products comprising such an extract of Isochrysis sp., preferably Tahitian Isochrysis.

EXTRACTS OF TETRASELMIS SP.

-

, (2010/06/19)

The present invention relates to extracts of Tetraselmis sp., preferably Tetraselmis suecica, its cosmetic, dermatological and/or therapeutic uses and compositions and cosmetic, dermatological or therapeutic products comprising such an extract of Tetraselmis sp., preferably Tetraselmis suecica.

Extracts of Tetraselmis sp. for cosmetic and therapeutic purposes

-

, (2010/06/20)

The present invention relates to extracts of Tetraselmis sp., preferably Tetraselmis suecica, its cosmetic, dermatological and/or therapeutic uses and compositions and cosmetic, dermatological or therapeutic products comprising such an extract of Tetraselmis sp., preferably Tetraselmis suecica.

Dynamic kinetic asymmetric transformation of 1,4-diols and the preparation of trans-2,5-disubstituted pyrrolidines

Borén, Linnéa,Leijondahl, Karin,B?ckvall, Jan-E.

supporting information; experimental part, p. 3237 - 3240 (2009/08/17)

Dynamic kinetic asymmetric transformation (DYKAT) of a series of 1,4-diols is carried out with Candida antarctica lipase B (CALB), Pseudomonas cepacia lipase II (PS-C II), and a ruthenium catalyst. A β-chloro-substituted 1,4-diol is successfully transformed into an optically pure 1,4-diacetate, which is a highly useful synthetic intermediate. The usefulness of the optically pure 1,4-diacetates is demonstrated by the synthesis of enantiopure 2,5-disubstituted pyrrolidines.

Nitroalkanes in Aqueous Medium as an Efficient and Eco-Friendly Source for the One-Pot Synthesis of 1,4-Diketones, 1,4-Diols, δ-Nitroalkanols, and Hydroxytetrahydrofurans

Ballini, Roberto,Barboni, Luciano,Giarlo, Guido

, p. 9173 - 9176 (2007/10/03)

The Michael addition of primary aliphatic nitro compounds to α,β-unsaturated enones, performed in aqueous media, provides the one-pot synthesis of 1,4-diketones, 1,4-diols, δ-nitroalkanols, and hydroxytetrahydrofurans, respectively, by the appropriate cho

Oxazaborolidine-catalysed reduction of alk-2-ene-1,4-diones. A convenient access to chiral 1,4-diols

Bach, Jordi,Berenguer, Ramon,Garcia, Jordi,Lopez, Marta,Manzanal, Judith,Vilarrasa, Jaume

, p. 14947 - 14962 (2007/10/03)

An efficient method for the preparation of C2-symmetric, chiral alk-2- ene-1,4-diols (4) has been achieved, based on the borane-mediated reduction of symmetric alk-2-ene-1,4-diones (2) in the presence of oxazaborolidine (R)- 1. In general, the presence of the double bond in 2 has been beneficial (compared with the related saturated 1,4-diketones 3) not only as far as the stereoselectivity in the reduction step is concerned, but also because it allowed us to remove meso-4 by chomatography and/or to improve the stereochemical purity of several resulting mixtures of diols 4 by Sharpless' epoxidation. Enantioenricbed compounds 4 have been readily reduced to saturated diols with negligible loss of optical purity.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 24434-09-1