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1310729-91-9

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1310729-91-9 Usage

General Description

3-Bromo-1,1-difluoro-cyclopropane is a chemical compound with the molecular formula C3H3BrF2. It is a halogenated organic compound that consists of a three-membered cyclopropane ring with bromine and fluorine atoms attached. 3-BroMo-1,1-difluoro-cycl... is used in chemical synthesis and research, particularly in the field of organic chemistry. It is known for its unique structural properties and reactivity, making it a valuable building block for the creation of other organic compounds. Additionally, its halogen substituents make it a useful reagent in various reactions, including nucleophilic substitution and ring-opening reactions. Overall, 3-Bromo-1,1-difluoro-cyclopropane is a significant compound in the realm of organic chemistry and is utilized for its distinctive chemical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 1310729-91-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,0,7,2 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1310729-91:
(9*1)+(8*3)+(7*1)+(6*0)+(5*7)+(4*2)+(3*9)+(2*9)+(1*1)=129
129 % 10 = 9
So 1310729-91-9 is a valid CAS Registry Number.

1310729-91-9Downstream Products

1310729-91-9Relevant articles and documents

Multigram Synthesis of C 4/C5 3,3-Difluorocyclobutyl-Substituted Building Blocks

Melnykov, Kostiantyn P.,Granat, Dmitriy S.,Volochnyuk, Dmitriy M.,Ryabukhin, Sergey V.,Grygorenko, Oleksandr O.

, p. 4949 - 4957 (2018/12/13)

An approach for the multigram synthesis of 3,3-difluorocyclobutyl-substituted building blocks (including carboxylic acid, amines, alcohols, azide, trifluoroborate ketone) is described. It is shown that, in most cases, ethyl 3,3-difluorocyclobutanecarboxylate is a convenient common synthetic intermediate to obtain the target derivatives. For preparation of 3,3-difluorocyclobutanol or -cyclobutanone, an alternative pathway via reaction of dichloroketene and tert -butyl or benzyl vinyl ether should be applied.

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