50915-29-2 Usage
Description
(1-bromocyclopropyl)methanol is a chemical compound that consists of a cyclopropyl ring and a hydroxyl group attached to a bromine atom. It is a type of organobromine compound and is commonly used in organic synthesis and medicinal chemistry.
Uses
Used in Pharmaceutical Industry:
(1-bromocyclopropyl)methanol is used as a building block for the synthesis of pharmaceuticals, as it can be incorporated into the molecular structure of various drugs. Its unique chemical properties allow it to be used in the development of new medications with specific therapeutic effects.
Used in Agrochemical Industry:
(1-bromocyclopropyl)methanol is used as a precursor in the production of agrochemicals, such as pesticides and herbicides. Its reactivity and ability to form stable compounds make it a valuable component in the creation of effective agricultural chemicals.
Used in Organic Synthesis:
(1-bromocyclopropyl)methanol is used as a reagent in organic synthesis for the preparation of various organic compounds. Its versatility in forming different types of chemical bonds allows it to be used in a wide range of chemical reactions, leading to the formation of diverse organic molecules.
It is important to handle (1-bromocyclopropyl)methanol with caution, as bromine compounds can be toxic and harmful to human health and the environment. Proper safety measures and protocols should be followed when working with this compound to ensure safe handling and disposal.
Check Digit Verification of cas no
The CAS Registry Mumber 50915-29-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,9,1 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 50915-29:
(7*5)+(6*0)+(5*9)+(4*1)+(3*5)+(2*2)+(1*9)=112
112 % 10 = 2
So 50915-29-2 is a valid CAS Registry Number.
50915-29-2Relevant articles and documents
Thermally induced [2+2] cycloadditions of (benzyloxymethylene)cyclopropane with alkylidenemalononitriles
Nakamura, Itaru,Nagata, Ryoko,Nemoto, Tetsuya,Terada, Masahiro,Yamamoto, Yoshinori,Spaeth, Thomas,De Meijere, Armin
, p. 4479 - 4482 (2008/02/12)
The reaction of (benzyloxymethylene)cyclopropane (1a) with alkylidenemalononitriles 2 at ambient pressure afforded the corresponding cyclobutane derivatives 3 in good-to-high yields. For example, the reaction of 1a with benzylidenemalononitrile (2a), (2-n
