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About This Item
Empirical Formula (Hill Notation):
C4H2Cl2N2
CAS Number:
Molecular Weight:
148.98
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
225-460-1
MDL number:
Assay:
95%
InChI key
MLCNOCRGSBCAGH-UHFFFAOYSA-N
InChI
1S/C4H2Cl2N2/c5-3-4(6)8-2-1-7-3/h1-2H
SMILES string
Clc1nccnc1Cl
assay
95%
density
1.431 g/mL at 25 °C (lit.)
functional group
chloro
Application
Selective monosubstitution of this substrate provided an efficient synthesis of alloisines, potent cyclin-dependent kinases.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
215.6 °F - closed cup
flash_point_c
102 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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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)
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