37632-18-1 Usage
Uses
Used in Pharmaceutical Industry:
4-Methoxyphenylphosphonic dichloride is used as an intermediate in the synthesis of various pharmaceuticals for its ability to form key chemical bonds and contribute to the development of new drugs.
Used in Agrochemical Industry:
4-Methoxyphenylphosphonic dichloride is used as an intermediate in the synthesis of agrochemicals to help create effective pesticides and other agricultural products that protect crops and enhance yields.
Used in Organic Compounds Synthesis:
4-Methoxyphenylphosphonic dichloride is used as a versatile intermediate in the synthesis of various organic compounds, enabling the creation of a wide range of chemical products for different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 37632-18-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,6,3 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 37632-18:
(7*3)+(6*7)+(5*6)+(4*3)+(3*2)+(2*1)+(1*8)=121
121 % 10 = 1
So 37632-18-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H7Cl2O2P/c1-11-6-2-4-7(5-3-6)12(8,9)10/h2-5H,1H3
37632-18-1Relevant academic research and scientific papers
N-hydroxylamines: Influence of Substituents on the Competitive Migration of Aryl and Phenyl Groups in the Lossen-like Rearrangement of their O-Methanesulphonyl Derivatives
Harger, Martin J. P.,Smith, Adrian
, p. 1787 - 1792 (2007/10/02)
The N-hydroxylamines ArPhP(O)NHOH (4) (Ar=p-XC6H4; X=MeO, Me, Cl, NO2) have been prepared from the corresponding phosphinic chlorides (3) using O-(trimethylsilyl)hydroxylamine and converted into the O-methanesulphonyl derivatives
SYNTHESIS OF PHOSPHONIC DICHLORIDES AND CORRELATION OF THEIR P-31 CHEMICAL SHIFTS
Grabiak, Raymond C.,Miles, James A.,Schwenzer, Gretchen M.
, p. 197 - 202 (2007/10/02)
Various mono-substituted diethyl arylphosphonates were prepared in good yield by treatment of aryl bromides or iodides with triethyl phosphite in the presence of NiCl2 or alternatively, addition of the aryl grignard reagent to diethyl phosphorochloridate.