Home Bromides 10075-50-0
10075-50-0,MFCD00005670
Catalog No.:AA0002PO
10075-50-0 | 5-Bromoindole
Pack Size
Purity
Availability
Price(USD)
Quantity
  
10g
97%
in stock  
$10.00   $7.00
- +
25g
97%
in stock  
$18.00   $12.00
- +
100g
98%
in stock  
$57.00   $40.00
- +
500g
98%
in stock  
$215.00   $150.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Q & A
  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA0002PO
Chemical Name:
5-Bromoindole
CAS Number:
10075-50-0
Molecular Formula:
C8H6BrN
Molecular Weight:
196.0439
MDL Number:
MFCD00005670
IUPAC Name:
5-bromo-1H-indole
InChI:
InChI=1S/C8H6BrN/c9-7-1-2-8-6(5-7)3-4-10-8/h1-5,10H
InChI Key:
VXWVFZFZYXOBTA-UHFFFAOYSA-N
SMILES:
Brc1ccc2c(c1)cc[nH]2
EC Number:
233-208-7
NSC Number:
75581
Properties
Computed Properties
 
Complexity:
126  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
194.968g/mol
Formal Charge:
0
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
0
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
196.047g/mol
Monoisotopic Mass:
194.968g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
15.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3  

Synonyms
 
5-BROMOINDOLE 
10075-50-0 
5bromoindole 
5-bromo-indole 
NSC75581 
EINECS 233-208-7 
NSC 75581 
zlchem 227 
5-bromo 1H indole 
PubChem1661 
5-Bromo-1H-indole # 
AC1L2NRD 
5-Bromo-1H-indole 
Maybridge1_006195 
ACMC-2097sd 
NCIOpen2_000472 
SCHEMBL74304 
KSC179K9N 
BIDD:GT0232 
5-BI 
AC1Q258P 
AMBZ0191 
Jsp000159 
1H-Indole, 5-bromo- 
DTXSID6073996 
CTK0H9596 
HMS559B13 
ZINC81120 
1H-Indole, 5-bromo- (9CI) 
ZLC0035 
ACN-P001097 
ACT02545 
ALBB-021314 
BCP26677 
5-bromo indole 
CS-D0617 
KS-000004ZE 
ANW-14363 
BBL013012 
BDBM50358747 
CCG-42502 
GEO-00480 
NSC-75581 
SBB054557 
STK249656 
MFCD00005670 
AKOS000120596 
AB00482 
AC-1348 
AN-1021 
FS-1805 
MCULE-7541905570 
RL00057 
RP04026 
RTC-060683 
TRA0074129 
5-Bromoindole, 99% 
AJ-10541 
AK-31145 
B2310G25 
BC002200 
BC200873 
BR-31145 
CJ-00656 
SC-00054 
SY005268 
ZB002881 
CHEMBL325917 
AB0051712 
AB1000409 
DB-012391 
ST2418686 
TC-060683 
AM20060209 
FT-0084524 
FT-0620159 
FT-0620160 
ST50330596 
VXWVFZFZYXOBTA-UHFFFAOYSA-N 
TL80073616 
MFCD00005670 (99%) 
75B500 
C-1025 
SR-01000632498-1 
F8881-6102 
InChI=1/C8H6BrN/c9-7-1-2-8-6(5-7)3-4-10-8/h1-5,10 
null 
5-bromine indole 
C8H6BrN 
220310-64-5 
C8-H6-Br-N 
CID24905 
ACN-028398 
2-AMINO-5-CHLORO-3-IODOPYRIDINE 
5-Bromoindole, 99% - 100G 100g 
B1738 
A16225 
B-8420 
B-8424 
18650-39-0 
Literature

Title: Identification of novel CYP2A6 inhibitors by virtual screening.

Journal: Bioorganic & medicinal chemistry 20111201

Title: Biocatalysed halogenation of nucleobase analogues.

Journal: Biotechnology letters 20111001

Title: Evaluation of novel aminomethyl indole derivatives as Src kinase inhibitors and antioxidant agents.

Journal: Chemotherapy 20110101

Title: Synthesis and anticancer activity of 5-(3-indolyl)-1,3,4-thiadiazoles.

Journal: European journal of medicinal chemistry 20101001

Title: 1-[(E)-4-(5-Bromo-1H-indol-3-yl)-1-methyl-2,5,6,7-tetra-hydro-1H-azepin-2-yl-idene]propan-2-one.

Journal: Acta crystallographica. Section E, Structure reports online 20100701

Title: 1H NMR spectral studies on the polymerization mechanism of indole and its derivatives.

Journal: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20060301

Title: Prediction of genotoxicity of chemical compounds by statistical learning methods.

Journal: Chemical research in toxicology 20050601

Title: Improved synthesis of aryltrialkoxysilanes via treatment of aryl Grignard or lithium reagents with tetraalkyl orthosilicates.

Journal: The Journal of organic chemistry 20041126

Title: Generation of new protein kinase inhibitors utilizing cytochrome p450 mutant enzymes for indigoid synthesis.

Journal: Journal of medicinal chemistry 20040603

Title: Hydroxylation of indole by laboratory-evolved 2-hydroxybiphenyl 3-monooxygenase.

Journal: The Journal of biological chemistry 20020913

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