7005-37-0

Basic information

• Product Name: 3,4-DIAMINO-BENZAMIDE
• Synonyms: 3,4-DIAMINO-BENZAMIDE;Benzamide, 3,4-diamino-
• CAS NO: 7005-37-0
• Molecular Formula: C₇H₉N₃O
• Molecular Weight: 151.16586
• Mol File: 7005-37-0.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 359.728°C at 760 mmHg
• Flash Point: 171.358°C
• Appearance: /
• Density: 1.341g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.702
• PKA: 17.08±0.50(Predicted)
• CAS DataBase Reference: 3,4-DIAMINO-BENZAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-DIAMINO-BENZAMIDE(7005-37-0)
• EPA Substance Registry System: 3,4-DIAMINO-BENZAMIDE(7005-37-0)

Safety Data

• Hazardous Substances Data: 7005-37-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C7H9N3O/c8-5-2-1-4(7(10)11)3-6(5)9/h1-3H,8-9H2,(H2,10,11)

Upstream product

• 41263-65-4 4-amino-3-nitrobenzamide 
• 17626-40-3 4-cyano-1,2-phenylenediamine 
• 1588-83-6 4-amino-3-nitrobenzoic acid 

Downstream Products

• 516481-11-1 2-[4-(3-carboxy-phenoxy)-phenyl]-1H-benzoimidazole-5-carboxylic acid amide 
• 1197338-11-6 C₂₂H₂₃N₇O₃ 
• 1197337-72-6 C₂₁H₂₁N₅O₄ 

Relevant articles and documents

BENZOTHIOPHENE, THIENOPYRIDINE AND THIENOPYRIMIDINE DERIVATIVES FOR THE MODULATION OF STING

A compound of formula (I); wherein: W is O or NH; A1 1 is CRAA or N; A22 is CRBB or N; A3A3 is CRCC or N; A44 is CRDD or N; where no more than two of A11, A

STING AGONISTS AND USES THEREOF

The present invention provides compounds, compositions thereof, and methods of using the same for the modulation of STING, and the treatment of STING-mediated disorders.

Monomeric nickel hydroxide stabilized by a sterically demanding phosphorus-nitrogen PN3P-pincer ligand: synthesis, reactivity and catalysis

A terminal nickel hydroxide complex (PN3P)Ni(OH) (3) bearing the 2nd generation phosphorus-nitrogen PN3P-pincer ligand has been synthesized and structurally characterized. As a nucleophile, 3 reacts with CO to afford the hydroxycarbonyl complex 4, (PN3P)Ni(COOH). 3 can also activate CO2 and CS2 to produce nickel bicarbonate (PN3P)Ni(OCOOH) (5) and bimetallic dithiocarbonate [(PN3P)NiS]2CO (6) respectively, as well as to promote aryl isocyanate and isothiocyanate insertion into the Ni-OH bond to give the corresponding (PN3P)NiEC(O)NHAr complexes (E = O, 7; E = S, 8). In addition, 3 catalyzes the nitrile hydration to various amides with well-defined intermediates (PN3P)Ni-NHC(O)R (R = Me, 9; R = Ph, 10).