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Home Other Building Blocks 1-Iodo-2-methylbenzene

1-Iodo-2-methylbenzene

CAS No.:
615-37-2
Catalog Number:
AG003HH1
Molecular Formula:
C7H7I
Molecular Weight:
218.0350
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
98%
In Stock USA
United States
$13
- +
25g
98%
In Stock USA
United States
$19
- +
100g
98%
In Stock USA
United States
$63
- +
500g
98%
In Stock USA
United States
$275
- +
Product Description
Catalog Number:
AG003HH1
Chemical Name:
1-Iodo-2-methylbenzene
CAS Number:
615-37-2
Molecular Formula:
C7H7I
Molecular Weight:
218.0350
MDL Number:
MFCD00001042
IUPAC Name:
1-iodo-2-methylbenzene
InChI:
InChI=1S/C7H7I/c1-6-4-2-3-5-7(6)8/h2-5H,1H3
InChI Key:
RINOYHWVBUKAQE-UHFFFAOYSA-N
SMILES:
Cc1ccccc1I
EC Number:
210-422-9
UNII:
8OK4H85T07
NSC Number:
3774
Properties
Complexity:
70.8  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
217.959g/mol
Formal Charge:
0
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
0
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
218.037g/mol
Monoisotopic Mass:
217.959g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
0A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.9  
Literature
Title Journal
Mizoroki-heck-type reaction mediated by potassium tert-butoxide. Angewandte Chemie (International ed. in English) 20110509
Spin-orbit ab initio investigation of photolysis of o-, m-, and p-iodotoluene. The Journal of chemical physics 20100107
Structures, biological activities, and total syntheses of 13-hydroxy- and 13-acetoxy-14-nordehydrocacalohastine, novel modified furanoeremophilane-type sesquiterpenes from Trichilia cuneata. Organic letters 20050428
Characterization of the electrophile binding site and substrate binding mode of the 26-kDa glutathione S-transferase from Schistosoma japonicum. Proteins 20030401
Synthesis of seven-membered lactones via nickel- and zinc-catalyzed highly regio- and stereoselective cyclization of 2-iodobenzyl alcohols with propiolates. Journal of the American Chemical Society 20020522
Properties