39804-96-1 Usage
Physical state
White solid the compound appears as a white solid in its pure form.
Melting point
78-80°C the temperature range at which the compound transitions from a solid to a liquid state.
Boiling point
290-295°C the temperature range at which the compound transitions from a liquid to a gas state.
Chemical classification
Urea derivative the compound is derived from urea, which is a functional group containing carbonyl groups on both ends.
Industrial and scientific applications
Used as an intermediate in the production of pesticides, pharmaceuticals, and other organic compounds the compound serves as a starting material or building block in the synthesis of various products.
Toxicity
Low toxicity the compound is not considered highly toxic or harmful to living organisms.
Environmental impact
Not harmful to the environment the compound is not known to cause significant negative effects on the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 39804-96-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,8,0 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 39804-96:
(7*3)+(6*9)+(5*8)+(4*0)+(3*4)+(2*9)+(1*6)=151
151 % 10 = 1
So 39804-96-1 is a valid CAS Registry Number.
39804-96-1Relevant articles and documents
A nonpeptidic reverse-turn scaffold stabilized by urea-based dual intramolecular hydrogen bonding
Medda, Amiya K.,Park, Chul Min,Jeon, Aram,Kim, Hyunwoo,Sohn, Jeong-Hun,Lee, Hee-Seung
supporting information; experimental part, p. 3486 - 3489 (2011/09/12)
A novel nonpeptidic reverse-turn scaffold containing urea fragments that are connected by a conformationally constrained d-prolyl-cis-1,2- diaminocyclohexane (d-Pro-DACH) linker is reported. The scaffold adopts a well-defined reverse-turn conformation tha
Electronic and Steric Effects of Alkyl Group on Denitrosation of 3-Alkyl-1-methyl-1-nitrosothioureas
Isobe, Masayoshi
, p. 2844 - 2848 (2007/10/02)
A series of 3-alkyl-1-methyl-1-nitrosothioureas with R=CH3, C2H5, cyclo-C6H11 (3), (CH3)2CH (4), C2H5(CH3)CH, and (CH3)3C were synthesized and their rates of acid catalyzes (pHH:kD is 1.25 for 4.Except 3, a linear plot of log kR/kMe for the denitrosation of RNHCSN(NO)CH3 vs. ?* provides ρ*=-0.98(r=-0.997).The significant factor affecting the rate determining step of the denitrosation of these N-nitrosothioureas at pH 4.6 is the electronic effect of the substituent at the N3 position.
