Cevoglitazar

Base Information

Chemical Name:Cevoglitazar
CAS No.:839673-52-8
Molecular Formula:C27H21F3N2O6S
Molecular Weight:558.535
Hs Code.:
UNII:6D0JK5KM96
DSSTox Substance ID:DTXSID301004208
Nikkaji Number:J2.595.803I
Wikidata:Q27264526
NCI Thesaurus Code:C81695

Synonyms:Cevoglitazar;Cevoglitazar [INN];839673-52-8;UNII-6D0JK5KM96;6D0JK5KM96;(R)-1-((4-((5-methyl-2-(4-(trifluoromethyl)phenyl)oxazol-4-yl)methoxy)phenyl)sulfonyl)indoline-2-carboxylic acid;SCHEMBL181098;KVVODNUBDFULSC-XMMPIXPASA-N;DTXSID301004208;AKOS040748111;Q27264526;(2R)-1-((4-((5-METHYL-2-(4-(TRIFLUOROMETHYL)PHENYL)-1,3-OXAZOL-4-YL)METHOXY)PHENYL)SULFONYL)INDOLINE-2-CARBOXYLIC ACID;(2R)-1-[4-[[5-methyl-2-[4-(trifluoromethyl)phenyl]-1,3-oxazol-4-yl]methoxy]phenyl]sulfonyl-2,3-dihydroindole-2-carboxylic acid;1-[4-({5-Methyl-2-[4-(trifluoromethyl)phenyl]-1,3-oxazol-4-yl}methoxy)benzene-1-sulfonyl]-2,3-dihydro-1H-indole-2-carboxylic acid;1H-INDOLE-2-CARBOXYLIC ACID, 2,3-DIHYDRO-1-((4-((5-METHYL-2-(4-(TRIFLUOROMETHYL)PHENYL)-4-OXAZOLYL)METHOXY)PHENYL)SULFONYL)-, (2R)-

Suppliers and Price of Cevoglitazar

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

Total 1 raw suppliers

Chemical Property of Cevoglitazar

Chemical Property:

XLogP3:5.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:11
Rotatable Bond Count:7
Exact Mass:558.10724205
Heavy Atom Count:39
Complexity:960

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(N=C(O1)C2=CC=C(C=C2)C(F)(F)F)COC3=CC=C(C=C3)S(=O)(=O)N4C(CC5=CC=CC=C54)C(=O)O
Isomeric SMILES:CC1=C(N=C(O1)C2=CC=C(C=C2)C(F)(F)F)COC3=CC=C(C=C3)S(=O)(=O)N4[C@H](CC5=CC=CC=C54)C(=O)O

Technology Process of Cevoglitazar

There total 1 articles about Cevoglitazar 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:

: 920266-85-9
4-[5-methyl-2-(4-trifluoromethyl-phenyl)-oxazol-4-ylmethoxy]-benzenesulfonic acid chloride

: 98167-06-7,78348-24-0
(R)-(-)-2,3-Dihydro-1H-Indole-2-Carboxylic Acid

: 839673-52-8
Cevoglitazar

Guidance literature:: (R)-(-)-2,3-Dihydro-1H-Indole-2-Carboxylic Acid; With sodium hydroxide; In water; acetonitrile; at 15 - 20 ℃; for 0.5h;

4-[5-methyl-2-(4-trifluoromethyl-phenyl)-oxazol-4-ylmethoxy]-benzenesulfonic acid chloride; In water; acetonitrile; at 15 - 20 ℃; for 3h; pH=5.5;

With hydrogenchloride; In water; acetonitrile; pH=1 - 2; Product distribution / selectivity;