Home Halogens 2,4-Dichlorotoluene

2,4-Dichlorotoluene

CAS No.:
95-73-8
Catalog Number:
AG003FRV
Molecular Formula:
C7H6Cl2
Molecular Weight:
161.0285
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
95%
In Stock USA
United States
$13
- +
25g
95%
In Stock USA
United States
$19
- +
100g
95%
In Stock USA
United States
$50
- +
Product Description
Catalog Number:
AG003FRV
Chemical Name:
2,4-Dichlorotoluene
CAS Number:
95-73-8
Molecular Formula:
C7H6Cl2
Molecular Weight:
161.0285
MDL Number:
MFCD00000583
IUPAC Name:
2,4-dichloro-1-methylbenzene
InChI:
InChI=1S/C7H6Cl2/c1-5-2-3-6(8)4-7(5)9/h2-4H,1H3
InChI Key:
FUNUTBJJKQIVSY-UHFFFAOYSA-N
SMILES:
Clc1ccc(c(c1)Cl)C
EC Number:
202-445-8
UNII:
3S32N6LG3X
NSC Number:
8764
Properties
Complexity:
92.9  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
159.985g/mol
Formal Charge:
0
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
0
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
161.025g/mol
Monoisotopic Mass:
159.985g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
0A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
4.2  
Literature
Title Journal
α-Bromo-2,6-dichlorotoluene: molecular structure, vibrational spectroscopy, natural bond orbital analysis and NMR studies. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20120901
Measurement and theory of hydrogen bonding contribution to isosteric DNA base pairs. Journal of the American Chemical Society 20120215
Rapid and selective catalytic oxidation of secondary alcohols at room temperature by using (N-heterocyclic carbene)-ni(0) systems. Chemistry (Weinheim an der Bergstrasse, Germany) 20100618
Discovery of 4-amino-1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidine-4-carboxamides as selective, orally active inhibitors of protein kinase B (Akt). Journal of medicinal chemistry 20100311
Synthesis, cannabinoid receptor affinity, molecular modeling studies and in vivo pharmacological evaluation of new substituted 1-aryl-5-(1H-pyrrol-1-yl)-1H-pyrazole-3-carboxamides. 2. Effect of the 3-carboxamide substituent on the affinity and selectivity profile. Bioorganic & medicinal chemistry 20090801
Diethyl 2,6-(2,4-dichloro-phen-yl)-4,8-dioxo-2,3,6,7-tetra-hydro-1H,5H-2,3a,4a,6,7a,8a-hexa-azacyclo-penta-[def]fluorene-8b,8c-dicarboxyl-ate. Acta crystallographica. Section E, Structure reports online 20090401
Redox-active dinitrodiphenylthioethers against Leishmania: synthesis, structure-activity relationships and mechanism of action studies. Bioorganic & medicinal chemistry 20090115
Probing the active site tightness of DNA polymerase in subangstrom increments. Proceedings of the National Academy of Sciences of the United States of America 20051101
A series of nonpolar thymidine analogues of increasing size: DNA base pairing and stacking properties. The Journal of organic chemistry 20050318
Simultaneous toxicity and nutrient removals in simulated DEPHANOX (anaerobic/anoxic/oxic sequentials) process treating dinitrotoluene and trichlorotoluene. Water science and technology : a journal of the International Association on Water Pollution Research 20040101
Metabolism of dichloromethylcatechols as central intermediates in the degradation of dichlorotoluenes by Ralstonia sp. strain PS12. Journal of bacteriology 20021001
Antimicrobial activity of 5-arylidene aromatic derivatives of hydantoin. Part 2. Farmaco (Societa chimica italiana : 1989) 20020101
Properties