130995-39-0 Usage
Description
(S)-4,5-ISOPROPYLIDENE-1-BROMOPENTANE, also known as isopropyldenebromopentane, is a chemical compound with the molecular formula C8H15Br. It is a colorless liquid with a slightly sweet odor and is characterized by its ability to form carbon-carbon bonds, making it a versatile building block in organic chemistry reactions.
Uses
Used in Pharmaceutical Industry:
(S)-4,5-ISOPROPYLIDENE-1-BROMOPENTANE is used as a reagent for the synthesis of various pharmaceutical compounds due to its ability to act as a versatile building block in organic chemistry reactions.
Used in Agrochemical Industry:
(S)-4,5-ISOPROPYLIDENE-1-BROMOPENTANE is used as a reagent in the preparation of agrochemicals, contributing to the development of new compounds for agricultural applications.
Used in Research and Development:
(S)-4,5-ISOPROPYLIDENE-1-BROMOPENTANE is used as a key component in the creation of complex molecular structures, playing a significant role in the research and development of new chemical compounds.
Safety Precautions:
It is important to handle (S)-4,5-ISOPROPYLIDENE-1-BROMOPENTANE with caution, as it is considered hazardous. It should be used in a well-ventilated area with appropriate personal protective equipment to ensure safety during its application in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 130995-39-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,9,9 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 130995-39:
(8*1)+(7*3)+(6*0)+(5*9)+(4*9)+(3*5)+(2*3)+(1*9)=140
140 % 10 = 0
So 130995-39-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H15Br/c1-8(2)6-7(8)4-3-5-9/h7H,3-6H2,1-2H3/t7-/m0/s1
130995-39-0Relevant articles and documents
Side-chain hydrophobicity controls the activity of proton channel forming rigid rod-shaped polyols
Ni, Chiyou,Matile, Stefan
, p. 755 - 756 (2007/10/03)
Increased activity, facile incorporation into lipid bilayers and intact active structure and transport selectivity are the consequences of modifications of the side-chain hydro-phobicity of a proton channel-forming octa(p-phenylene).
