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(2R,3R,4S)-1-Benzyloxy-2,4-dimethyl-hex-5-en-3-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

124377-68-0

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124377-68-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124377-68-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,3,7 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 124377-68:
(8*1)+(7*2)+(6*4)+(5*3)+(4*7)+(3*7)+(2*6)+(1*8)=130
130 % 10 = 0
So 124377-68-0 is a valid CAS Registry Number.

124377-68-0Downstream Products

124377-68-0Relevant academic research and scientific papers

STEREOCHEMICAL CONSEQUENCES FOR THE LEWIS ACID MEDIATED ADDITIONS OF ALLYL AND CROTYLTRI-n-BUTYLSTANNANE TO CHIRAL β-HYDROXYALDEHYDE DERIVATIVES

Keck, Gary E.,Abbott, Duain E.

, p. 1883 - 1886 (1984)

Proper choice of Lewis acid and hydroxyl protecting group allows for selective addition of crotyltri-n-butylstannane to either face of the aldehyde carbonyl in derivatives of 2-methyl-3-hydroxypropanal with preservation of erythro selectivity for the bond

Effects of Plefin Geometry on the Stereochemistry of Lewis Acid Mediated Additions of Crotylstannanes to Aldehydes

Keck, Gary E.,Savin, Kenneth A.,Cressman, Erik N. K.,Abbott, Duane E.

, p. 7889 - 7896 (2007/10/02)

The role of the double bond geometry (E/Z stereochemistry) in reactions of crotylstannanes with aldehydes has been examined for representative "simple", α-alkoxy, and β-alkoxy aldehydes.For the reaction of crotylstannane with simple achiral aliphatic, aro

CROTYLZIRCONIUM DERIVATIVES AS A NEW REAGENT FOR THE THREO SELECTIVE SYNTHESIS OF β-METHYLHOMOALLYL ALCOHOLS

Yamamoto, Yoshinori,Maruyama, Kazuhiro

, p. 2895 - 2898 (2007/10/02)

Crotylzirconium derivatives, prepared from the reaction of crotylmagnesium chloride or crotyllithium with bis(cyclopentadienyl)zirconium dichloride, undergo a rapid reaction with aldehydes to afford the threo product predominantly.The ratio of Cram/anti-Cram product via this reagent is ca. 75/25 ca. 60/40.

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