92192-94-4 Usage
General Description
1-Benzhydryl-2-thiourea, also known as BHTU, is a chemical compound with the molecular formula C20H20N2S. It is a synthetic organic compound that has a variety of applications, including as a fungicide and a rubber accelerator. BHTU is a white crystalline solid that is soluble in organic solvents but insoluble in water. It is commonly used in the rubber industry to accelerate the vulcanization process and improve the overall properties of rubber products. Additionally, BHTU has also been used as a fungicide in agriculture to control various fungal diseases. However, its use has raised concerns about its potential environmental and health impacts, and it is important to handle and dispose of it properly to minimize these risks.
Check Digit Verification of cas no
The CAS Registry Mumber 92192-94-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,1,9 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92192-94:
(7*9)+(6*2)+(5*1)+(4*9)+(3*2)+(2*9)+(1*4)=144
144 % 10 = 4
So 92192-94-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H14N2S/c15-14(17)16-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10,13H,(H3,15,16,17)
92192-94-4Relevant articles and documents
Tricyclic compounds, their production and use
-
, (2008/06/13)
A compound of the formula: wherein R1 is H or a substituent; m is 1-3; Ar is an aromatic group which may be substituted; X is a bond or a divalent straight-chain group having 1-6 atoms which may be substituted; Y is —S—, —O—, or —N(R2— (R2 is H or a substituent group), Z is —N= or —C(R3)= (R3 is H or a hydrocarbon group), ring A is a benzene ring; ring B is a 5- to 7-membered ring which may be substituted, or a salt thereof is useful for eliciting a prostaglandin I2 receptor agonistic effect.
N,N'-disubstituted guanidine high-potency sweeteners
Muller,Walters,DuBois
, p. 740 - 743 (2007/10/02)
The role and function of the aryl group in the highly potent trisubstituted guanidine sweeteners 7a-d was investigated. Four disubstituted guanidines, lacking the aryl group, were prepared. These guanidines contain a hydrophobic substituent on one nitroge