27329-60-8 Usage
General Description
DIETHYL(DIPHENYLMETHYL) PHOSPHATE, also known as DDVP or dichlorvos, is a highly toxic and potentially harmful chemical compound commonly used as an insecticide and pesticide. It is a clear, colorless liquid with a strong odor and is typically used to control a wide range of insect pests in agricultural, residential, and industrial settings. DDVP works by inhibiting the enzyme acetylcholinesterase, leading to the accumulation of acetylcholine and causing paralysis and ultimately death in the targeted insects. However, DDVP is also considered a potential human carcinogen and has been linked to a range of health issues, including respiratory, cardiovascular, and neurological effects. Due to its high toxicity and potential risks, the use of DIETHYL(DIPHENYLMETHYL) PHOSPHATE has become increasingly restricted in many countries.
Check Digit Verification of cas no
The CAS Registry Mumber 27329-60-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,3,2 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 27329-60:
(7*2)+(6*7)+(5*3)+(4*2)+(3*9)+(2*6)+(1*0)=118
118 % 10 = 8
So 27329-60-8 is a valid CAS Registry Number.
InChI:InChI=1/C17H21O3P/c1-3-19-21(18,20-4-2)17(15-11-7-5-8-12-15)16-13-9-6-10-14-16/h5-14,17H,3-4H2,1-2H3
27329-60-8Relevant articles and documents
Preparation method of large-steric-hindrance alkyl substituted phosphite diester
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Paragraph 0024-0027, (2020/04/06)
The invention discloses a preparation method of large-steric-hindrance alkyl substituted phosphite diester, and relates to a novel method for preparing the large-steric-hindrance alkyl substituted phosphite diester compound which is difficult to synthesiz
Oxidative Dephosphorylation of Benzylic Phosphonates with Dioxygen Generating Symmetrical trans-Stilbenes
Huang, Tianzeng,Chen, Tieqiao,Han, Li-Biao
, p. 2959 - 2965 (2018/03/09)
Under a dioxygen atmosphere, benzylphosphonates and related phosphoryl compounds can readily produce the corresponding trans-stilbenes in high yields with high selectivity upon treatment with bases. Various functional groups were tolerable under the reaction conditions.
Palladium-catalyzed α-arylation of benzylic phosphonates
Montel, Sonia,Raffier, Ludovic,He, Yuying,Walsh, Patrick J.
, p. 1446 - 1449 (2014/04/03)
A new synthetic route to access diarylmethyl phosphonates is presented. The transformation enables the introduction of aromatic groups on benzylic phosphonates via a deprotonative cross-coupling process (DCCP). The Pd(OAc) 2/CataCXium A-based catalyst afforded a reaction between benzyl diisopropyl phosphonate derivatives and aryl bromides in good to excellent isolated yields (64-92%).
