s-Triazine, 2-amino-4-(p-(propylthio)anilino)-

Base Information

Chemical Name:s-Triazine, 2-amino-4-(p-(propylthio)anilino)-
CAS No.:1087-33-8
Molecular Formula:C₁₂H₁₅N₅S
Molecular Weight:261.351
Hs Code.:
NSC Number:19755
UNII:9JW7BLT8RJ
DSSTox Substance ID:DTXSID60148715
Nikkaji Number:J92.229C
Wikidata:Q83014314
Mol file:1087-33-8.mol

Synonyms:s-Triazine, 2-amino-4-(p-(propylthio)anilino)-;1087-33-8;2-N-(4-propylsulfanylphenyl)-1,3,5-triazine-2,4-diamine;9JW7BLT8RJ;NSC-19755;N2-(4-(Propylthio)phenyl)-1,3,5-triazine-2,4-diamine;NSC 19755;BRN 0750907;2-Amino-4-(p-(propylthio)anilino)-s-triazine;NSC19755;2-Amino-4-(4-propylmercaptophenylamino)-1,3,5-triazine;UNII-9JW7BLT8RJ;DTXSID60148715;1,3,5-TRIAZINE-2,4-DIAMINE, N2-(4-(PROPYLTHIO)PHENYL)-

Suppliers and Price of s-Triazine, 2-amino-4-(p-(propylthio)anilino)-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
S-TRIAZINE, 2-AMINO-4-(P-(PROPYLTHIO)ANILINO)- 95.00%
5MG
$ 495.14

Total 9 raw suppliers

Chemical Property of s-Triazine, 2-amino-4-(p-(propylthio)anilino)-

Chemical Property:

Vapor Pressure:6.46E-10mmHg at 25°C
Boiling Point:494.4°Cat760mmHg
Flash Point:252.8°C
Density:1.28g/cm³
XLogP3:2.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:5
Exact Mass:261.10481667
Heavy Atom Count:18
Complexity:233

Purity/Quality:

98%,99%, ^*data from raw suppliers

S-TRIAZINE, 2-AMINO-4-(P-(PROPYLTHIO)ANILINO)- 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCSC1=CC=C(C=C1)NC2=NC=NC(=N2)N

Technology Process of s-Triazine, 2-amino-4-(p-(propylthio)anilino)-

There total 1 articles about s-Triazine, 2-amino-4-(p-(propylthio)anilino)- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: