75885-60-8 Usage
Uses
Used in Pharmaceutical Industry:
2,2-Dichlorocyclopropane-1-carboxamide is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique cyclopropane ring structure allows for the development of new drugs with distinct properties and therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical industry, 2,2-Dichlorocyclopropane-1-carboxamide serves as an essential intermediate for the production of various agrochemicals. Its reactivity and stability contribute to the creation of effective pesticides and other agricultural chemicals that can enhance crop protection and yield.
Used in Organic Synthesis:
2,2-Dichlorocyclopropane-1-carboxamide is utilized as a versatile building block in organic synthesis. Its cyclopropane ring can be further modified or used as a starting point for the synthesis of a wide range of organic compounds, including specialty chemicals and advanced materials.
Check Digit Verification of cas no
The CAS Registry Mumber 75885-60-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,8,8 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 75885-60:
(7*7)+(6*5)+(5*8)+(4*8)+(3*5)+(2*6)+(1*0)=178
178 % 10 = 8
So 75885-60-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H5Cl2NO/c5-4(6)1-2(4)3(7)8/h2H,1H2,(H2,7,8)
75885-60-8Relevant academic research and scientific papers
Thienamycin renal peptidase inhibitors
-
, (2008/06/13)
Novel chemical compounds are provided which selectively inhibit the metabolism of dipeptidase (E.C.3.4.13.11) and therefore are useful in combination with antibacterial products. These chemical compounds are z-2-acylamino-3-monosubstituted propenoates.
NUCLEOPHILIC SUBSTITUTION OF HALOGEN ATOMS IN gem-DICHLOROCYCLOPROPANES ACTIVATED BY ELECTRON-WITHDRAWING SUBSTITUENTS
Kulinkovich, O. G.,Tishchenko, I. G.,Romashin, Yu. N.
, p. 213 - 216 (2007/10/02)
The reactions of the methyl ester, N,N-dimethylamide, and nitrile of gem-dichlorocyclopropanecarboxylic acid with sodium methoxide and ethoxide take place with opening of the three-membered ring and lead to the correponding derivatives of succinic acid.Methyl and ethyl 3-formyl-2-methylpropionate were obtained from 2,2-dichloro-1-formyl-3-methylcyclopropane under analogous conditions.The reaction of sodium thiophenolate with the functionally substituted gem-dichlorocyclopropanes takes place with retention of the three-membered ring and the formation of the corresponding substituted diphenyl thioacetals of cyclopropanone.
