403735-05-7 Usage
Description
(S)-1-BOC-2-CHLOROMETHYL-PYRROLIDINE is a pyrrolidine derivative with the molecular formula C10H18ClNO2. It features a BOC (tert-butoxycarbonyl) protecting group and a chloromethyl group attached to the pyrrolidine ring, making it a versatile intermediate in organic synthesis.
Uses
Used in Pharmaceutical Industry:
(S)-1-BOC-2-CHLOROMETHYL-PYRROLIDINE is used as a key intermediate in the synthesis of various drugs and pharmaceutical compounds. Its unique structure allows for the development of new medications with potential therapeutic benefits.
Used in Agrochemical Manufacturing:
(S)-1-BOC-2-CHLOROMETHYL-PYRROLIDINE is also utilized in the production of agrochemicals, contributing to the development of effective products for agricultural applications and crop protection.
Used in Dye Production:
(S)-1-BOC-2-CHLOROMETHYL-PYRROLIDINE serves as an important building block in the synthesis of dyes, enabling the creation of a wide range of colorants for various industries.
Used in Fine Chemicals Synthesis:
(S)-1-BOC-2-CHLOROMETHYL-PYRROLIDINE is employed in the manufacturing of other fine chemicals, showcasing its broad applicability in the chemical industry for producing specialty products.
Check Digit Verification of cas no
The CAS Registry Mumber 403735-05-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,3,7,3 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 403735-05:
(8*4)+(7*0)+(6*3)+(5*7)+(4*3)+(3*5)+(2*0)+(1*5)=117
117 % 10 = 7
So 403735-05-7 is a valid CAS Registry Number.
403735-05-7Relevant articles and documents
Triphosgene-amine base promoted chlorination of unactivated aliphatic alcohols
Villalpando, Andres,Ayala, Caitlan E.,Watson, Christopher B.,Kartika, Rendy
, p. 3989 - 3996 (2013/06/04)
Unactivated α-branched primary and secondary aliphatic alcohols have been successfully transformed into their corresponding alkyl chlorides in high yields upon treatment with a mixture of triphosgene and pyridine in dichloromethane at reflux. These mild chlorination conditions are high yielding, stereospecific, and well tolerated by numerous sensitive functionalities. Furthermore, no nuisance waste products are generated in the course of the reactions.
An efficient route to alkyl chlorides from alcohols using the complex TCT/DMF
De Luca, Lidia,Giacomelli, Giampaolo,Porcheddu, Andrea
, p. 553 - 555 (2007/10/03)
(formula presented) Efficient conversion of alcohols and β-amino alcohols to the corresponding chlorides (and bromides) can be carried out at room temperature in methylene chloride, using 2,4,6-trichloro[1,3,5]triazine and N,N-dimethyl formamide. This procedure can also be applied to optically active carbinols.
