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1008-65-7,MFCD00020713
Catalog No.:AA0002UM
1008-65-7 | 2-(1,3,4-Oxadiazol-2-yl)phenol
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1g
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5g
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10g
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  • Technical Information
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  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA0002UM
Chemical Name:
2-(1,3,4-Oxadiazol-2-yl)phenol
CAS Number:
1008-65-7
Molecular Formula:
C8H6N2O2
Molecular Weight:
162.1454
MDL Number:
MFCD00020713
IUPAC Name:
2-(1,3,4-oxadiazol-2-yl)phenol
InChI:
InChI=1S/C8H6N2O2/c11-7-4-2-1-3-6(7)8-10-9-5-12-8/h1-5,11H
InChI Key:
OINXXHYENYVYPB-UHFFFAOYSA-N
SMILES:
Oc1ccccc1c1nnco1
UNII:
8YX6HIZ0IP
NSC Number:
100729
Properties
Computed Properties
 
Complexity:
154  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
162.043g/mol
Formal Charge:
0
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
162.148g/mol
Monoisotopic Mass:
162.043g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
59.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.1  

Synonyms
 
2-(1,3,4-Oxadiazol-2-yl)phenol 
1008-65-7 
J. L. 512 
2-(1,3,4-oxadiazol-2-yl)benzenol 
2-(o-Hydroxyphenyl)-1,3,4-oxadiazole 
Fenadiazole [INN:DCF] 
UNII-8YX6HIZ0IP 
Fenadiazol [INN-Spanish] 
Fenadiazolum [INN-Latin] 
NSC 100729 
PHENOL, 2-(1,3,4-OXADIAZOL-2-YL)- 
1,3,4-Oxadiazole, 2-(o-hydroxyphenyl)- 
Fenadiazole 
8YX6HIZ0IP 
Phenol, o-1,3,4-oxadiazol-2-yl- 
BRN 0136925 
MLS002703546 
OINXXHYENYVYPB-UHFFFAOYSA-N 
JL-512 
MFCD00020713 
ACMC-1BZDH 
AC1NSE2D 
AC1NTGD2 
Fenadiazol 
AC1O9VRQ 
DSSTox_CID_31397 
DSSTox_RID_97283 
DSSTox_GSID_57608 
4-27-00-07344 (Beilstein Handbook Reference) 
o-1,4-Oxadiazol-2-ylphenol 
SCHEMBL555484 
Phenol,3,4-oxadiazol-2-yl- 
AC1Q788K 
IFLab1_006238 
Eudormil 
IFLab2_000252 
ZINC1423 
CHEMBL1903897 
DTXSID7057608 
Phenol,3,4-oxadiazol-2-yl)- 
CTK3J6765 
KS-00001QCH 
o-1,3,4-Oxodiazol-2-ylphenol 
2-(1,4-Oxadiazol-2-yl)phenol 
CHEBI:134791 
Hypnazol 
HMS1429L12 
Tox21_113759 
0284AA 
ANW-55011 
NSC100729 
ODZ100103 
SBB041007 
STK409833 
2-(o-Hydroxyphenyl)-1,4-oxadiazole 
ortho-1,3,4-Oxadiazol-2-yl-phenol 
Viodor 
2-(1,3,4-Oxadiazol-2-yl)-phenol 
AKOS000269733 
MCULE-5839956801 
NE32146 
NSC-100729 
RP10242 
RTR-000262 
SDCCGMLS-0065586.P001 
IDI1_019278 
1,4-Oxadiazole, 2-(o-hydroxyphenyl)- 
Fenadiazolum 
2-(2-hydroxyphenyl)-1,3,4-oxadiazole 
NCGC00253631-01 
AJ-08024 
SMR001570263 
ZB000331 
ZB000332 
CAS-1008-65-7 
DB-058510 
LS-105017 
TR-000262 
JL 512 
FT-0608353 
Phenol, o-1,3,4-oxadiazol-2-yl- (8CI) 
ST24039033 
ST50107712 
10A-002 
AT-057/42646623 
J-505292 
BRD-K18362446-001-06-8 
I01-15995 
6-(3H-1,3,4-oxadiazol-2-ylidene)cyclohexa-2,4-dien-1-one 
o-1,3,4-Oxadiazol-2-ylphenol 
(6E)-6-(3H-1,3,4-oxadiazol-2-ylidene)cyclohexa-2,4-dien-1-one 
(6Z)-6-(3H-1,3,4-oxadiazol-2-ylidene)cyclohexa-2,4-dien-1-one 
Fenadiazole [DCF:INN] 
C8H6N2O2 
C8-H6-N2-O2 
CID5359546 
CID5380573 
CID6738087 
Literature

Title: Efficient Electrochemical Synthesis, Antimicrobial and Antiinflammatory Activity of 2-amino-5-substituted- 1,3,4-oxadiazole Derivatives.

Journal: Indian journal of pharmaceutical sciences 20100101

Title: Synthesis, Antimicrobial and Antiinflammatory Activity of 2,5-Disubstituted-1,3,4-oxadiazoles.

Journal: Indian journal of pharmaceutical sciences 20080101

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