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3-Hexanone, 1-hydroxy-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54135-69-2

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54135-69-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54135-69-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,1,3 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 54135-69:
(7*5)+(6*4)+(5*1)+(4*3)+(3*5)+(2*6)+(1*9)=112
112 % 10 = 2
So 54135-69-2 is a valid CAS Registry Number.

54135-69-2Downstream Products

54135-69-2Relevant academic research and scientific papers

Catalytic Conjunctive Coupling of Carboxylic Acid Derivatives with 9-BBN-Derived Ate Complexes

Law, Chunyin,Meng, Yan,Koo, Seung Moh,Morken, James P.

, p. 6654 - 6658 (2019)

β-Boryl carbonyl compounds are produced by a Ni-catalyzed cross-coupling of vinylboron “ate” complexes and acid chloride or acid anhydride electrophiles. The reactions are efficient, being complete in as little as two minutes, and can be applied to a broad range of substrates.

Crossed aldol reaction using cross-linked polymer-bound lithium dialkylamide

Seki, Atsushi,Ishiwata, Fusae,Takizawa, Youichi,Asami, Masatoshi

, p. 5001 - 5011 (2007/10/03)

Cross-linked polymer-bound lithium dialkylamides were employed in crossed aldol reaction of various carbonyl compounds with aldehydes to afford the corresponding β-hydroxycarbonyl compounds. The introduction of spacer chains to the polymer-bound lithium d

Crossed aldol reaction using polymer-bound lithium amides

Seki, Atsushi,Takizawa, Youichi,Ishiwata, Fusae,Asami, Masatoshi

, p. 342 - 343 (2007/10/03)

Polymer-bound lithium amides were used in an aldol reaction. The introduction of a spacer between the polymer backbone and the reactive site was important to enhance yields of the aldol products. The polymer-bound reagent was repeatedly used in the same r

Lewis acid-promoted cross aldol reaction of aldehydes with ketones utilizing 3-methyl-2-phenyl-2-(2-oxoalkyl)benzothiazolines as an enolate-transferring reagent

Chikashita,Tame -i.,Yamada,Itoh

, p. 497 - 501 (2007/10/02)

The treatment of a variety of 3-methyl-2-phenyl-2-(2-oxoalkyl) benzothiazolines with aldehydes in the presence of 2 equivalents of SnCl4 in dichloromethane at -78°C underwent a carbon-carbon bond cleavage at the 2-position of the benzothiazolin

NOVEL ALDOL-TYPE REACTION UTILIZING 3-METHYL-2-PHENYL-2-(2-OXOALKYL)BENZOTHIAZOLINE AS AN ENOLATE TRANSFERRING REAGENT

Chikashita, Hidenori,Tame, Shin-ichiro,Itoh, Kazuyoshi

, p. 67 - 70 (2007/10/02)

An enolate transfer-type aldol reaction of the title benzothiazoline with aldehydes was successfully achieved in the presence of SnCl4 to afford the cross aldol products.

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