All Photos(1)
About This Item
Empirical Formula (Hill Notation):
C4H2Cl2N2
CAS Number:
Molecular Weight:
148.98
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
95%
density
1.431 g/mL at 25 °C (lit.)
functional group
chloro
SMILES string
Clc1nccnc1Cl
InChI
1S/C4H2Cl2N2/c5-3-4(6)8-2-1-7-3/h1-2H
InChI key
MLCNOCRGSBCAGH-UHFFFAOYSA-N
Application
Selective monosubstitution of this substrate provided an efficient synthesis of alloisines, potent cyclin-dependent kinases.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
215.6 °F - closed cup
Flash Point(C)
102 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
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.
Steven R Kennedy et al.
Inorganic chemistry, 55(4), 1433-1445 (2016-01-27)
We demonstrate that protonation of a mixed valence molecule, generating a mixed valence mixed protonated (MVMP) state, results in a severe reduction in the electronic coupling intimately connected with electron transfer kinetics. This phenomenon is illustrated by synthesizing a mixed
Tetrahedron, 62, 9919-9919 (2006)
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