741493
1,2-Diamino-3,5-dimethylbenzene
96%
Synonym(s):
3,5-Dimethyl-1,2-phenylenediamine
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About This Item
Empirical Formula (Hill Notation):
C8H12N2
CAS Number:
Molecular Weight:
136.19
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
96%
Form:
solid
InChI
1S/C8H12N2/c1-5-3-6(2)8(10)7(9)4-5/h3-4H,9-10H2,1-2H3
SMILES string
Cc1cc(C)c(N)c(N)c1
InChI key
DMEPVFSJYHJGCD-UHFFFAOYSA-N
assay
96%
form
solid
mp
73-78 °C
storage temp.
2-8°C
Quality Level
Related Categories
Application
1,2-Diamino-3,5-dimethylbenzene can be used as a starting material to synthesize:
- Tetramethyl quinoxaline derivatives by reacting with 1,2-dicarbonyl compounds.
- 5,7-Dimethyl-1H-benzotriazole by reacting with tert-butyl nitrite.
- Dimethyl-1H-benzimidazole by reacting with dimethylformamide (DMF).
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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A Facile, Catalyst-Free Mechano-Synthesis of Quinoxalines and their In-Vitro Antibacterial Activity Study
Bhutia ZT, et al.
ChemistrySelect, 2(3), 1183-1187 (2017)
Expedient synthesis of benzimidazoles using amides
Kattimani PP, et al.
Royal Society of Chemistry Advances, 5(37), 29447-29455 (2015)
tert-Butyl nitrite mediated nitrogen transfer reactions: synthesis of benzotriazoles and azides at room temperature
Azeez S, et al.
Organic & Biomolecular Chemistry, 16(37), 8280-8285 (2018)
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