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3,6,7-trimethyl-2,6-octadien-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42933-32-4

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42933-32-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42933-32-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,9,3 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 42933-32:
(7*4)+(6*2)+(5*9)+(4*3)+(3*3)+(2*3)+(1*2)=114
114 % 10 = 4
So 42933-32-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H20O/c1-9(2)11(4)6-5-10(3)7-8-12/h7,12H,5-6,8H2,1-4H3/b10-7+

42933-32-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2E)-3,6,7-trimethylocta-2,6-dien-1-ol

1.2 Other means of identification

Product number -
Other names EINECS 256-009-7

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:42933-32-4 SDS

42933-32-4Relevant academic research and scientific papers

Rerouting and Improving Dauc-8-en-11-ol Synthase from Streptomyces venezuelae to a High Yielding Biocatalyst

Lauterbach, Lukas,Hou, Anwei,Dickschat, Jeroen S.

, p. 7923 - 7929 (2021/04/21)

The dauc-8-en-11-ol synthase from Streptomyces venezuelae was investigated for its catalytic activity towards alternative terpene precursors, specifically designed to enable new cyclisation pathways. Exchange of aromatic amino acid residues at the enzyme surface by site-directed mutagenesis led to a 4-fold increase of the yield in preparative scale incubations, which likely results from an increased enzyme stability instead of improved enzyme kinetics.

SELECTIVE HYDROGENATION OF ALDEHYDE WITH RU/BIDENTATE LIGANDS COMPLEXES

-

Paragraph 0189, (2014/09/03)

The present invention relates to processes for the reduction by hydrogenation, using molecular H2, of a C5-C20 substrate containing one or two aldehydes functional groups into the corresponding alcohol or diol, characterized in that said process is carried out in the presence of —at least one catalyst or pre-catalyst in the form of a ruthenium complex having a coordination sphere of the N2P2O2, wherein the coordinating atoms N2 are provided by a first bidentate ligand, the coordinating atoms P2 are provided by a second bidentate ligand and the coordinating atoms O2 are provided by two non-linear carboxylate ligands; and —optionally of an acidic additive.

Synthesis of teleocidins A, B and their congeners. Part 3. Synthesis of dihydroteleocidin B-4 (dihydroteleocidin B), teleocidin B-3 and teleocidin B-4

Okabe, Kazuaki,Muratake, Hideaki,Natsume, Mitsutaka

, p. 8559 - 8572 (2007/10/02)

Details of the synthesis method of the tumor promoters teleocidin B-3 (3), teleocidin B-4 (4) and dihydroteleocidin B-4 (9) (=dihydroteleocidin B) from (S)- and (R)-methyl N-methyl-N-[7-(3,6,7-trimethyl-1,6-octadien-3-yl)-4-indolyl]-L-valinates (20b and 20a) are presented.

TOTAL SYNTHESES OF (+/-)-β-IRONE

Moiseenkov, A. M.,Veselovskii, V. V.,Dragan, V. A.,Stashina, G. A.,Zhulin, V. M.

, p. 2394 - 2397 (2007/10/02)

The conversion of the product of the ene reaction of PhSOCl with geranyl acetate into racemic β-irone has been accomplished in seven steps, using high-pressure techniques for the olefination of β-methylcyclocitral.

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