Thiamine disulfide phosphate

Base Information

Chemical Name:Thiamine disulfide phosphate
CAS No.:992-46-1
Molecular Formula:C₂₄H₃₆N₈O₁₀P₂S₂
Molecular Weight:722.677
Hs Code.:
UNII:HIX040UVAZ
Wikidata:Q27279948

Synonyms:Thiamine disulfide phosphate;Biotinin;Vitamogen;Thiamine monophosphate disulfide;HIX040UVAZ;992-46-1;Tmpds;Thiamine disulfide phosphate (JAN);THIAMINE DISULFIDE PHOSPHATE [JAN];UNII-HIX040UVAZ;Thiamine-O-monophosphate disulfide;BRN 0077276;4-25-00-02932 (Beilstein Handbook Reference);SCHEMBL642270;THIAMINE DISULFIDE PHOSPHATE [MI];THIAMINE DISULFIDE PHOSPHATE [WHO-DD];D04933;Q27279948;Formamide, N,N'-(dithiobis(1-methyl-2-(2-(phosphonooxy)ethyl)-2,1-ethanediyl))bis(N-((4-amino-2-methyl-5-pyrimidinyl)methyl)-;FORMAMIDE, N,N'-(DITHIOBIS(1-METHYL-2-(2-(PHOSPHONOOXY)ETHYL)-2,1-ETHENEDIYL))BIS(N-((4-AMINO-2-METHYL-5-PYRIMIDINYL)METHYL)-;Formamide, N,N'-(dithiobis(2-(2-hydroxyethyl)-1-methylvinylene))bis(N-((4-amino-2-methyl-5-pyrimidinyl)methyl)-, bis(dihydrogen phosphate) (ester)

Suppliers and Price of Thiamine disulfide phosphate

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of Thiamine disulfide phosphate

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Boiling Point:1055.4°Cat760mmHg
Flash Point:592.1°C
Density:1.552g/cm³
XLogP3:-2.7
Hydrogen Bond Donor Count:6
Hydrogen Bond Acceptor Count:18
Rotatable Bond Count:17
Exact Mass:722.14710572
Heavy Atom Count:46
Complexity:1090

Purity/Quality:

Safty Information:

Pictogram(s):
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MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCOP(=O)(O)O)SSC(=C(C)N(CC2=CN=C(N=C2N)C)C=O)CCOP(=O)(O)O)C
Isomeric SMILES:CC1=NC=C(C(=N1)N)CN(/C(=C(\SS/C(=C(\N(C=O)CC2=CN=C(N=C2N)C)/C)/CCOP(=O)(O)O)/CCOP(=O)(O)O)/C)C=O

Technology Process of Thiamine disulfide phosphate

There total 4 articles about Thiamine disulfide phosphate 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: