1224174-07-5 Usage
Description
(S)-1-chlorohept-6-en-2-ol, with the molecular formula C7H13ClO, is a chiral chemical compound that exists as a colorless liquid. It has a molecular weight of 148.63 g/mol and is characterized by its non-superimposable mirror image, which is a feature of chiral compounds. (S)-1-chlorohept-6-en-2-ol is known for its utility in organic synthesis and serves as a versatile intermediate in the creation of a wide range of organic compounds.
Uses
Used in Pharmaceutical Industry:
(S)-1-chlorohept-6-en-2-ol is used as an intermediate in the synthesis of various pharmaceuticals. Its unique structure and properties make it a valuable building block for the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
(S)-1-chlorohept-6-en-2-ol is also utilized as an intermediate in the production of agrochemicals. Its role in the synthesis of various agrochemical products highlights its versatility and importance in the agricultural sector.
Used in Fragrance Industry:
(S)-1-chlorohept-6-en-2-ol is employed in the fragrance industry as an intermediate for creating different types of scents. Its contribution to the development of new fragrances adds to its significance in the industry.
Safety Precautions:
It is crucial to handle (S)-1-chlorohept-6-en-2-ol with care due to its toxic nature. Exposure to this compound can cause irritation to the skin, eyes, and respiratory system. Proper safety measures should be taken to minimize the risk of adverse health effects.
Check Digit Verification of cas no
The CAS Registry Mumber 1224174-07-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,4,1,7 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1224174-07:
(9*1)+(8*2)+(7*2)+(6*4)+(5*1)+(4*7)+(3*4)+(2*0)+(1*7)=115
115 % 10 = 5
So 1224174-07-5 is a valid CAS Registry Number.
1224174-07-5Relevant articles and documents
Asymmetric Synthesis of Functionalized trans-Cyclopropoxy Building Block for Grazoprevir
Xu, Feng,Zhong, Yong-Li,Li, Hongming,Qi, Ji,Desmond, Richard,Song, Zhiguo J.,Park, Jeonghan,Wang, Tao,Truppo, Matthew,Humphrey, Guy R.,Ruck, Rebecca T.
, p. 5880 - 5883 (2017)
A practical and asymmetric synthesis of a functionalized trans-cyclopropoxy building block for the preparation of the HCV NS3/4a protease inhibitor grazoprevir is reported. Intramolecular SN2 displacement-ring closure, followed by a Baeyer-Villiger oxidation, yields the desired trans-cyclopropanol with full control of diastereoselectivity. A terminal alkyne is then effectively installed using LiNH(CH2)2NEt2. Starting from (S)-epichlorohydrin, the cyclopropoxy building block is prepared in 51% overall yield with >99.8% optical purity without isolation of any intermediates.
METHODS AND INTERMEDIATES FOR PREPARING MACROLACTAMS
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Page/Page column 24, (2015/05/05)
The present invention includes compounds useful as intermediates in the preparation of macrolactams, methods for preparing the intermediates, and methods for preparing macrolactams. One use of the methods and intermediates described herein is in the production of macrolactam compounds able to inhibit HCV NS3 protease activity. HCV NS3 inhibitory compounds have therapeutic and research applications.
