139165-54-1 Usage
Description
1,4-Dichlorobutane-2S-3S-diol, with the CAS number 139165-54-1, is a brown solid compound that is primarily utilized in the field of organic synthesis. Its unique chemical structure and properties make it a valuable component in the creation of various organic compounds.
Uses
Used in Organic Synthesis:
1,4-Dichlorobutane-2S-3S-diol is used as a key intermediate in the synthesis of various organic compounds. Its chemical properties allow it to be a versatile building block for the development of new molecules with potential applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1,4-Dichlorobutane-2S-3S-diol is used as a starting material for the synthesis of new drugs. Its unique structure can be modified to create novel drug candidates with potential therapeutic effects.
Used in Chemical Research:
1,4-Dichlorobutane-2S-3S-diol is also used in chemical research to study the reactivity and behavior of different functional groups. This knowledge can be applied to develop new synthetic methods and improve existing ones.
Used in Material Science:
In the field of material science, 1,4-Dichlorobutane-2S-3S-diol can be used to develop new materials with specific properties. Its unique structure can be incorporated into polymers or other materials to enhance their performance.
Check Digit Verification of cas no
The CAS Registry Mumber 139165-54-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,1,6 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 139165-54:
(8*1)+(7*3)+(6*9)+(5*1)+(4*6)+(3*5)+(2*5)+(1*4)=141
141 % 10 = 1
So 139165-54-1 is a valid CAS Registry Number.
139165-54-1Relevant articles and documents
Asymmetric Dihydroxylation of Primary Allylic Halides and a Concise Synthesis of (-)-Diepoxybutane
Vanhessche, Koen P. M.,Wang, Zhi-Min,Sharpless, K. Barry
, p. 3469 - 3472 (1994)
The asymmetric dihydroxylation (AD) of primary allylic halides is described.Enantiomeric excesses range from 40 to 98percent.Subsequent base treatment gives epoxy alcohols in high yields.This strategy is further illustrated by the synthesis of (-)-diepoxybutane, an important C4-chiral building block.
Catalytic Asymmetric Dihydroxylation of Aliphatic Olefins with Reusable Resin-Osmium Tetroxide
Choudary, Boyapati M.,Jyothi, Karangula,Madhi, Sateesh,Kantam, M. Lakshmi
, p. 1190 - 1192 (2007/10/03)
Asymmetric dihydroxylation of aliphatic olefins to chiral diols with good yields and ees by a heterogeneous Resin-OsO4 catalyst using ferricyanide as cooxidant is disclosed for the first time. The catalyst was recovered quantitatively by simple filtration and reused for several times without significant loss of activity.
Synthesis of a chiral aziridine derivative as a versatile intermediate for HIV protease inhibitors.
Kim,Bae,So,Yoo,Chang,Lee,Kang
, p. 2349 - 2351 (2007/10/03)
[reaction: see text] Chiral aziridine derivative 1 was prepared from D-tartaric acid. This compound could be utilized as a common intermediate for the synthesis of hydroxyethylamine class HIV protease inhibitors such as saquinavir, amprenavir, or nelfinavir.
