741493
1,2-Diamino-3,5-dimethylbenzene
96%
Synonym(s):
3,5-Dimethyl-1,2-phenylenediamine
Sign In to View Organizational & Contract Pricing.
Select a Size
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
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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)
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)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service