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1-phenyl-3-cyclopropyl-3-buten-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

144729-95-3

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144729-95-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144729-95-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,7,2 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 144729-95:
(8*1)+(7*4)+(6*4)+(5*7)+(4*2)+(3*9)+(2*9)+(1*5)=153
153 % 10 = 3
So 144729-95-3 is a valid CAS Registry Number.

144729-95-3Downstream Products

144729-95-3Relevant academic research and scientific papers

Cooperative titanocene and phosphine catalysis: Accelerated C-X activation for the generation of reactive organometallics

Fleury, Lauren M.,Kosal, Andrew D.,Masters, James T.,Ashfeld, Brandon L.

, p. 253 - 269 (2013/03/14)

The study presented herein describes a reductive transmetalation approach toward the generation of Grignard and organozinc reagents mediated by a titanocene catalyst. This method enables the metalation of functionalized substrates without loss of functional group compatibility. Allyl zinc reagents and allyl, vinyl, and alkyl Grignard reagents were generated in situ and used in the addition to carbonyl substrates to provide the corresponding carbinols in yields up to 99%. It was discovered that phosphine ligands effectively accelerate the reductive transmetalation event to enable the metalation of C-X bonds at temperatures as low as -40 °C. Performing the reactions in the presence of chiral diamines and amino alcohols led to the enantioselective allylation of aldehydes.

Synthesis and Reactions of 2-Cyclopropyl-2-propenyltrimethylsilane. Silicon-Directed Generation of Cyclopropylcarbinyl System

Hojo, Makoto,Ohsumi, Katsufumi,Hosomi, Akira

, p. 5981 - 5982 (2007/10/02)

2-Cyclopropyl-2-propenyltrimethylsilane reacts with various kinds of carbon electrophiles to afford the corresponding allylation products without contamination of other products based on the rearrangement of a cyclopropyl ring.

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