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41370-29-0

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41370-29-0 Usage

Color

Colorless

Physical state

Liquid

Uses

Building block in the synthesis of various organic compounds, production of fragrances, flavorings, and pharmaceuticals, solvent, intermediate in the manufacturing of other chemical products

Unique properties

Unique chemical structure

Versatility

Wide range of applications in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 41370-29-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,3,7 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 41370-29:
(7*4)+(6*1)+(5*3)+(4*7)+(3*0)+(2*2)+(1*9)=90
90 % 10 = 0
So 41370-29-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O/c1-10(2)6-3-4-9(8-10)5-7-11/h5,11H,3-4,6-8H2,1-2H3

41370-29-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3,3-dimethylcyclohexylidene)ethanol

1.2 Other means of identification

Product number -
Other names -

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:41370-29-0 SDS

41370-29-0Relevant articles and documents

Pheromone Synthesis, CXV. - Synthesis of (Z)-2-Ochtoden-1-ol, (E)-2-Ochtoden-1-al, and (Z)-2-Ochtoden-1-al, the Pheromone Components of the Boll Weevil (Anthonomus grandis)

Mori, Kenji,Itou, Masamichi

, p. 969 - 974 (2007/10/02)

The synthesis of geometrically pure (Z)-2-ochtoden-1-ol (1), (E)-2-ochtoden-1-al (2), and (Z)-2-ochtoden-1-al (3) was achieved starting from myrcene.

HIGHLY STEROSELECTIVE SYNTHESIS OF EXOCYCLIC ALKENES VIA CYCLIALKYLATION

Negishi, Ei-ichi,Zhang, Yantao,Bagheri, Vahid

, p. 5793 - 5796 (2007/10/02)

Treatment of stereodefined ω-halo-2-iodoalkene derivatives (1), prepared via stereoselective addition reactions of alkynes, with either n-BuLi (1 equiv) or t-BuLi (2 equiv) can produce exocyclic alkenes whose isomeric purity is essentially 100percent.

NEW OCHTODANE SYNTHESES FROM MYRCENE

Masaki, Yukio,Hashimoto, Kinji,Sakuma, Kazuhiko,Kaji, Kenji

, p. 1481 - 1484 (2007/10/02)

The ochtodane skeleton is formed stereoselectively from myrcene via acid-catalyzed cyclization of the benzenesulfenyl chloride adduct and the epoxide in a biogenetic type fashion.Its application to the syntheses of two ochtodane-type monoterpenes, an aldehyde component of the boll weevil pheromone and a diol found in the red alga Ochtodes crockeri, is reported.

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