17606-31-4 Usage
Description
Bensultap, also known as S,S-2-dimethylaminotrimethylene di(benzenethiosulfonate) (IUPAC), is a pale yellow crystalline powder with a molecular weight of 431.6 and the chemical formula C17H21NO4S4. It has limited solubility in water (0.7–0.8 mg/kg at 30°C) and high solubility in methanol (25 g/kg at 25°C), as well as in acetone, acetonitrile, and N,N-dimethylformamide (>1000 g/kg). Bensultap is hydrolyzed in neutral or alkaline solutions and acts as an insecticide with contact and stomach action for controlling major insect pests. It functions as a pro-insecticide or analog of nereistoxin, inhibiting the action of acetylcholine by blocking the receptor site at the post-synaptic membrane.
Uses
Used in Pesticide Industry:
Bensultap is used as an insecticide in pesticidal compositions for the control of major insect pests. It provides effective contact and stomach action, making it a valuable tool in agriculture for protecting crops from damaging insects.
Bensultap is used as a pro-insecticide or analog of nereistoxin for inhibiting the action of acetylcholine by blocking the receptor site at the post-synaptic membrane, which helps in controlling insect populations and reducing the impact of pests on crops.
Check Digit Verification of cas no
The CAS Registry Mumber 17606-31-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,0 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 17606-31:
(7*1)+(6*7)+(5*6)+(4*0)+(3*6)+(2*3)+(1*1)=104
104 % 10 = 4
So 17606-31-4 is a valid CAS Registry Number.
InChI:InChI=1/C17H21NO4S4/c1-18(2)15(13-23-25(19,20)16-9-5-3-6-10-16)14-24-26(21,22)17-11-7-4-8-12-17/h3-12,15H,13-14H2,1-2H3
17606-31-4Relevant articles and documents
Novel process for producing thiolsulfonic acid derivatives
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, (2008/06/13)
This invention relates to a process for producing a thiolsulfonic acid derivative of the general formula: STR1 wherein each of R1 and R2 is independently a lower alkyl group or a 5- or 6-membered cycloalkyl group, or alternatively R1 and R2 together with the adjacent nitrogen atom form a 5- or 6-membered heterocyclic group which may further contain an oxygen, sulfur or nitrogen atom; and R3 is (1) an aryl group which may optionally be substituted by a lower alkyl group, a halogen, a lower alkoxy group or a lower alkylthio group, (2) a lower alkyl group which may optionally be substituted by a lower alkoxy group, (3) an aralkyl group or (4) a cycloalkyl group, or a salt thereof, which comprises reacting a compound of the general formula: STR2 wherein R1 and R2 are as defined above, or a salt thereof with a compound of the general formula: wherein R3 is as defined above, or a salt thereof under an acid condition. The compound (I) or a salt thereof is produced in high purity and in high yield according to the process of this invention.