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39627-84-4,MFCD00016810
Catalog No.:AA003HOJ
39627-84-4 | 2-Naphthhydrazide
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1g
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$156.00
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5g
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Technical Information
Catalog Number:
AA003HOJ
Chemical Name:
2-Naphthhydrazide
CAS Number:
39627-84-4
Molecular Formula:
C11H10N2O
Molecular Weight:
186.2099
MDL Number:
MFCD00016810
IUPAC Name:
naphthalene-2-carbohydrazide
InChI:
InChI=1S/C11H10N2O/c12-13-11(14)10-6-5-8-3-1-2-4-9(8)7-10/h1-7H,12H2,(H,13,14)
InChI Key:
RARLPRMZJNIQGU-UHFFFAOYSA-N
SMILES:
NNC(=O)c1ccc2c(c1)cccc2
EC Number:
254-547-7
Properties
Computed Properties
 
Complexity:
217  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
186.079g/mol
Formal Charge:
0
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
186.214g/mol
Monoisotopic Mass:
186.079g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
55.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.3  

Synonyms
 
2-Naphthohydrazide 
2-Naphthhydrazide 
MFCD00016810 
2-naphthoylhydrazine 
EINECS 254-547-7 
zlchem 976 
2-Naphthohydrazide # 
beta-Naphthoylhydrazine 
AC1L3WOY 
AC1Q5PUF 
ACMC-1AFU5 
2-naphthoic acid hydrazide 
39627-84-4 
AC1Q54UU 
SCHEMBL1149678 
CTK1C2818 
DTXSID40192731 
ZLD0442 
ZINC323472 
ALBB-001063 
5202AB 
ANW-54886 
BBL001791 
naphthalene-2-carbohydrazide 
BDBM50320733 
SBB090426 
STK331010 
2-Naphthalenecarboxylicacid, hydrazide 
AKOS000143576 
FS-4780 
MCULE-8942978997 
VZ25021 
AJ-19254 
ZB010432 
2-naphthoic hydrazide 
AB0116134 
DB-021409 
TR-036698 
FT-0613118 
FT-0613120 
ST50825249 
EN300-44166 
C-5367 
AN-068/40771566 
I14-27409 
2-Naphthalenecarboxylic acid, hydrazide 
-naphthoylhydrazine 
C11H10N2O 
AR-1E4279 
C11-H10-N2-O 
CID123485 
ZINC00323472 
41451-70-1 
.beta.-Naphthoylhydrazine 
Naphthalene-2-carboxylic acid hydrazide 
CHEMBL153973 
RARLPRMZJNIQGU-UHFFFAOYSA-N 
Literature

Title: New potent inhibitors of tyrosinase: novel clues to binding of 1,3,4-thiadiazole-2(3H)-thiones, 1,3,4-oxadiazole-2(3H)-thiones, 4-amino-1,2,4-triazole-5(4H)-thiones, and substituted hydrazides to the dicopper active site.

Journal: Bioorganic & medicinal chemistry 20100601

Title: Aromatic hydroxamic acids and hydrazides as inhibitors of the peroxidase activity of prostaglandin H2 synthase-2.

Journal: Archives of biochemistry and biophysics 20041101

Title: Mechanism of horseradish peroxidase inactivation by benzhydrazide: a critical evaluation of arylhydrazides as peroxidase inhibitors.

Journal: The Biochemical journal 20031101

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