55117-15-2 Usage
Description
2-Chloro-6-fluorobenzyl chloride is an organic compound characterized by its clear colorless liquid appearance. It is a derivative of benzyl chloride, featuring a chlorine atom at the 2nd position and a fluorine atom at the 6th position on the benzene ring. 2-Chloro-6-fluorobenzyl chloride is known for its reactivity and is commonly utilized in various chemical synthesis processes.
Uses
Used in Pharmaceutical Industry:
2-Chloro-6-fluorobenzyl chloride is used as an alkylating reagent for the synthesis of 3-benzylsulfanyl derivatives of 1,2,4-triazole and 4-methyl-1,2,4-triazole. These derivatives are essential in the development of new pharmaceutical compounds with potential therapeutic applications.
Used in Chemical Synthesis:
In the preparation of 2-chloro-6-fluorobenzylamine, 2-chloro-6-fluorobenzyl chloride is used as a key intermediate. This amine compound is required for the synthesis of 9-substituted adenine, which is an important component in the development of various chemical and pharmaceutical products.
Used in the Synthesis of Aprinocid:
2-Chloro-6-fluorobenzyl chloride is also utilized in the preparation of aprinocid, a compound with potential applications in the field of medicine. The reaction of 2-chloro-6-fluorobenzyl chloride with adenine is a crucial step in the synthesis of aprinocid.
Overall, 2-chloro-6-fluorobenzyl chloride is a versatile compound with applications in various industries, particularly in the pharmaceutical and chemical synthesis sectors. Its unique chemical properties make it a valuable reagent in the development of new compounds and products.
Check Digit Verification of cas no
The CAS Registry Mumber 55117-15-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,1,1 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55117-15:
(7*5)+(6*5)+(5*1)+(4*1)+(3*7)+(2*1)+(1*5)=102
102 % 10 = 2
So 55117-15-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H9Cl/c1-7-4-2-3-5-8(7)6-9/h2-5H,6H2,1H3
55117-15-2Relevant articles and documents
[4,5]-fused-3,6-disubstituted-pyridazines with sulfur-containing substituents in position three for the treatment of neoplasia
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, (2008/06/13)
[4,5]-Fused-3,6 disubstituted-pydidazines of Formula I are useful for inducing or promoting apoptosis and for arresting uncontrolled neoplastic cell proliferation, and are specifically useful in the arresting and treatment of neoplasia: wherein Y1and Y2are independently selected from the group consisting of (CH2)n,—C(X)—NH—,—(CH2)n—C(X)—O—, and X is O or S; R1is selected from the group consisting of lower alkyl, lower alkenyl, lower alkynyl, and substituted or unsubstituted phenyl, pyridinyl, and the like; R2is selected from the group consisting of substituted or unsubstituted phenyl, benzyl, pyridinyl, and the like; “A” is a benzene ring fused with the pyridazine ring; and R3is independently selected in each instance form the group consisting of halogen, lower alkyl, and the like.
Synthesis of 1-methyl-1-(substituted benzyl)hydrazines.
Butler,Alexander,McLean,Strand
, p. 1052 - 1054 (2007/10/05)
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