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1-octylcyclohexanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5770-04-7

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5770-04-7 Usage

Physical state

Colorless to pale yellow liquid

Solubility

Insoluble in water

Odor

Mild, pleasant

Usage

Fragrance ingredient in personal care products (perfumes, lotions, soaps), solvent, intermediate in chemical production

Volatility

Low

Stability

Low

Toxicity

Low, considered safe for use in consumer products when used within regulatory guidelines

Check Digit Verification of cas no

The CAS Registry Mumber 5770-04-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,7 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5770-04:
(6*5)+(5*7)+(4*7)+(3*0)+(2*0)+(1*4)=97
97 % 10 = 7
So 5770-04-7 is a valid CAS Registry Number.

5770-04-7Relevant academic research and scientific papers

Organocalcium Chemistry: Preparation and Reactions of Highly Reactive Calcium

Wu, Tse-Chong,Xiong, Heping,Rieke, R. D.

, p. 5045 - 5051 (2007/10/02)

A highly reactive form of calcium was prepared by the reduction of Ca(II) salts with preformed lithium biphenylide.Remarkably, this activated calcium undergoes oxidative addition to organic bromides, chlorides, or even fluorides to form the organocalcium reagents under very mild conditions in high yields.The resulting organocalcium compounds undergo Grignard-type reactions.Transmetalation with Cu(I) salts forms calcium cuprate reagents which undergo a variety of cross-coupling reactions.The activated calcium reacts with 1,3-dienes to yield the corresponding 2-butene-1,4-diylcalcium complexes.These bis-organocalcium reagents can undergo dialkylation reactions with α,ω-alkylene dihalides and dichlorosilanes to form the corresponding 3-, 5-, and 6-membered ring derivatives.Significantly, these reactions are highly stereospecific and regioselective.

Deprotection of Tetrahydropyranyl and Silyl Ethers Catalyzed by Organotin Phosphate Condensates

Otera, Junzo,Niibo, Yoshihisa,Chikada, Sadamasa,Nozaki, Hitosi

, p. 328 - 329 (2007/10/02)

A new method for deprotecting tetrahydropyranyl and silyl ethers has been established by using organotin phosphate condensates as a catalyst.The reaction proceeds selectively under mild conditions.The heterogenous reaction enables easy separation of the catalyst, which can be reused for further reactions without purification.

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