ANTIPYRYLAZO III

Details

Stereochemistry	ACHIRAL
Molecular Formula	C32H28N8O10S2
Molecular Weight	748.742
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	2
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

CN1N(C(=O)C(\N=N\C2=C(O)C3=C(O)C(\N=N\C4=C(C)N(C)N(C4=O)C5=CC=CC=C5)=C(C=C3C=C2S(O)(=O)=O)S(O)(=O)=O)=C1C)C6=CC=CC=C6

InChI

InChIKey=SZVOKPKIXYMQHL-LBYUQGKWSA-N

InChI=1S/C32H28N8O10S2/c1-17-25(31(43)39(37(17)3)20-11-7-5-8-12-20)33-35-27-22(51(45,46)47)15-19-16-23(52(48,49)50)28(30(42)24(19)29(27)41)36-34-26-18(2)38(4)40(32(26)44)21-13-9-6-10-14-21/h5-16,41-42H,1-4H3,(H,45,46,47)(H,48,49,50)/b35-33+,36-34+

HIDE SMILES / InChI

Molecular Formula	C32H28N8O10S2
Molecular Weight	748.742
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	2
Optical Activity	NONE

Approval Year

Substance Class	Chemical Created by `admin` on `Mon Mar 31 23:42:01 GMT 2025` Edited by `admin` on `Mon Mar 31 23:42:01 GMT 2025`
Record UNII	H378L7UI14
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

ANTIPYRINE S

Preferred Name

English

ANTIPYRYLAZO III

Common Name

English

2,7-NAPHTHALENEDISULFONIC ACID, 3,6-BIS(ANTIPYRINYLAZO)-4,5-DIHYDROXY-

Systematic Name

English

2,7-NAPHTHALENEDISULFONIC ACID, 3,6-BIS(2-(2,3-DIHYDRO-1,5-DIMETHYL-3-OXO-2-PHENYL-1H-PYRAZOL-4-YL)DIAZENYL)-4,5-DIHYDROXY-

Systematic Name

English

2,7-NAPHTHALENEDISULFONIC ACID, 3,6-BIS((2,3-DIHYDRO-1,5-DIMETHYL-3-OXO-2-PHENYL-1H-PYRAZOL-4-YL)AZO)-4,5-DIHYDROXY-

Systematic Name

English

3,6-BIS((ANTIPYRINE)AZO)-4,5-DIHYDROXY-2,7-NAPHTHALENE DISULFONIC ACID

Systematic Name

English

DIANTIPYRYLAZO

Common Name

English

Code System Code Type Description

ECHA (EC/EINECS)

238-988-2

Created by admin on Mon Mar 31 23:42:01 GMT 2025 , Edited by admin on Mon Mar 31 23:42:01 GMT 2025

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CAS

14918-39-9

Created by admin on Mon Mar 31 23:42:01 GMT 2025 , Edited by admin on Mon Mar 31 23:42:01 GMT 2025

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EPA CompTox

DTXSID901104731

Created by admin on Mon Mar 31 23:42:01 GMT 2025 , Edited by admin on Mon Mar 31 23:42:01 GMT 2025

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FDA UNII

H378L7UI14

Created by admin on Mon Mar 31 23:42:01 GMT 2025 , Edited by admin on Mon Mar 31 23:42:01 GMT 2025

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