75885-60-8 Usage
General Description
2,2-Dichlorocyclopropane-1-carboxamide is a chemical compound which exists as a white solid at room temperature. It is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. 2,2-DICHLOROCYCLOPROPANE-1-CARBOXAMIDE is known for its cyclopropane ring structure, which confers unique reactivity and stability properties. It is important to handle and store this chemical with caution, as it is classified as hazardous due to its potential to cause skin and eye irritation, as well as respiratory issues if inhaled. Additionally, it is important to note that 2,2-Dichlorocyclopropane-1-carboxamide is typically produced under strictly controlled conditions to ensure its purity and safety for use in various industrial applications.
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 articles and documents
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.
