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1,3-Cyclohexadiene-1-methanol, 2,6,6-trimethyl- is an organic compound with the molecular formula C10H18O. It is a colorless liquid at room temperature and is characterized by its unique structure, which includes a cyclohexadiene ring with a methanol group attached to the first carbon and three methyl groups attached to the second, sixth, and sixth carbons, respectively. 1,3-Cyclohexadiene-1-methanol,2,6,6- trimethyl- is primarily used as an intermediate in the synthesis of various chemicals, particularly in the production of fragrances and pharmaceuticals. Due to its reactive nature, it is essential to handle 1,3-Cyclohexadiene-1-methanol,2,6,6- trimethyl- with care, following proper safety protocols to minimize potential health and environmental risks.

4436-51-5

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4436-51-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4436-51-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,3 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4436-51:
(6*4)+(5*4)+(4*3)+(3*6)+(2*5)+(1*1)=85
85 % 10 = 5
So 4436-51-5 is a valid CAS Registry Number.

4436-51-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-hydroxymethyl-2,6,6-trimethylcyclohexa-1,3-diene

1.2 Other means of identification

Product number -
Other names (2,6,6-trimethyl-cyclohexa-1,3-dienyl)-methanol

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:4436-51-5 SDS

4436-51-5Relevant academic research and scientific papers

154. Synthese von optisch aktiven, natuerlichen Carotinoiden und strukturell verwandten Naturprodukten. V. Synthese von (3R,3'R)-, (3S,3'S)- und (3R,3'S; meso)-Zeaxanthin durch asymmetrische Hydroborierung. Ein neuer Zugang zu optisch aktiven Carotinoidba

Ruettimann, August,Mayer, Hans

, p. 1456 - 1462 (1980)

The synthesis of (3R,3'R)-, (3S,3'S)- and (3R,3'S; meso)-zeaxanthin (1), (19) and (21) is reported utilizing asymmetric hydroboration as the key reaction.Thus, safranol isopropenylmethylether (4) is hydroborated with (+)- and (-)-(IPC)2BH to give the opti

Singlet oxygen addition to cyclo-1,3-hexadienes from natural sources and from organocatalytic enal dimerization

Griesbeck, Axel G.,De Kiff, Alan,Neud?rfl, J?rg M.,Sillner, Sarah

, p. 101 - 110 (2015/04/14)

The photoxygenation reactions of the natural monoterpene aldehyde safranal (1 ) and its reduction product safranol ( 4) were studied and the endoperoxide 5 from safranol was isolated and characterized by single crystal X-ray analysis. A dyade synthesis us

SYNTHESIS OF OPTICALLY ACTIVE 3-DIAZOACETYLRETINALS WITH TRIISOPROPYLPHENYLSULFONYLHYDRAZONE

Ok, Hyun,Caldwell, Charles,Schroeder, Daniel R.,Singh, Anil K.,Nakanishi, Koji

, p. 2275 - 2278 (2007/10/02)

An improved synthesis of photoaffinity labeled, optically active retinal derivatives is presented.A stable, easy to handle, glyoxalic acid 2,4,6-triisopropylphenylsulfonylhydrazone (TIPPS) reacts with 3-hydroxyretinal to give the diazoacetylretinal analog in satisfactory yield.

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