99277-23-3,MFCD06656049
Catalog No.:AA01B9JO

99277-23-3 | N'-hydroxybenzenecarboximidamide hydrochloride

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
95+%
2 weeks  
$53.00   $37.00
- +
5g
95+%
2 weeks  
$83.00   $58.00
- +
25g
95+%
2 weeks  
$232.00   $163.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA01B9JO
Chemical Name:
N'-hydroxybenzenecarboximidamide hydrochloride
CAS Number:
99277-23-3
Molecular Formula:
C7H9ClN2O
Molecular Weight:
172.6122
MDL Number:
MFCD06656049
SMILES:
ON=C(c1ccccc1)N.Cl
Properties
Computed Properties
 
Complexity:
128  
Covalently-Bonded Unit Count:
2  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
1  
Formal Charge:
0  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0  
Rotatable Bond Count:
1  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  

Downstream Synthesis Route
99277-23-3    74-86-2   
N'-(vinyloxy)benzenecarboximidamide 

[1]Trofimov;Schmidt;Vasil'Tsov;Mikhaleva;Zaitsev;Morozova;Gorshkov;Henkelmann;Arndt[Synthesis,2001,#16,p.2427-2430]

[1]Trofimov;Schmidt;Vasil'Tsov;Mikhaleva;Zaitsev;Morozova;Gorshkov;Henkelmann;Arndt[Synthesis,2001,#16,p.2427-2430]

Literature

Title: Insight into technetium amidoxime complex: oxo technetium(V) complex of N-substituted benzamidoxime as new basic structure for molecular imaging.

Journal: Inorganic chemistry 20110207

Title: Reduction of N(ω)-hydroxy-L-arginine by the mitochondrial amidoxime reducing component (mARC).

Journal: The Biochemical journal 20110115

Title: A novel and specific fluorescence reaction for uracil.

Journal: Analytica chimica acta 20100803

Title: The fourth molybdenum containing enzyme mARC: cloning and involvement in the activation of N-hydroxylated prodrugs.

Journal: Journal of medicinal chemistry 20081225

Title: Involvement of stearoyl-CoA desaturase in the reduction of amidoxime prodrugs.

Journal: Xenobiotica; the fate of foreign compounds in biological systems 20080901

Title: Identification of the missing component in the mitochondrial benzamidoxime prodrug-converting system as a novel molybdenum enzyme.

Journal: The Journal of biological chemistry 20061117

Title: Hepatic, extrahepatic, microsomal, and mitochondrial activation of the N-hydroxylated prodrugs benzamidoxime, guanoxabenz, and Ro 48-3656 ([[1-[(2s)-2-[[4-[(hydroxyamino)iminomethyl]benzoyl]amino]-1-oxopropyl]-4-piperidinyl]oxy]-acetic acid).

Journal: Drug metabolism and disposition: the biological fate of chemicals 20051101

Title: Characterization and partial purification of the rat and human enzyme systems active in the reduction of N-hydroxymelagatran and benzamidoxime.

Journal: Drug metabolism and disposition: the biological fate of chemicals 20050401

Title: Metabolism of benzamidoxime (N-hydroxyamidine) in human hepatocytes and role of UDP-glucuronosyltransferases.

Journal: Xenobiotica; the fate of foreign compounds in biological systems 20050101

Title: Phase 2 metabolites of N-hydroxylated amidines (amidoximes): synthesis, in vitro formation by pig hepatocytes, and mutagenicity testing.

Journal: Chemical research in toxicology 20010301

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SDS
Tags:99277-23-3 Molecular Formula|99277-23-3 MDL|99277-23-3 SMILES|99277-23-3 N'-hydroxybenzenecarboximidamide hydrochloride
Catalog No.: AA01B9JO
99277-23-3,MFCD06656049
99277-23-3 | N'-hydroxybenzenecarboximidamide hydrochloride
Pack Size: 1g
Purity: 95+%
2 weeks
$53.00 $37.00
Pack Size: 5g
Purity: 95+%
2 weeks
$83.00 $58.00
Pack Size: 25g
Purity: 95+%
2 weeks
$232.00 $163.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA01B9JO
Chemical Name: N'-hydroxybenzenecarboximidamide hydrochloride
CAS Number: 99277-23-3
Molecular Formula: C7H9ClN2O
Molecular Weight: 172.6122
MDL Number: MFCD06656049
SMILES: ON=C(c1ccccc1)N.Cl
Properties
Complexity: 128  
Covalently-Bonded Unit Count: 2  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 1  
Formal Charge: 0  
Heavy Atom Count: 11  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 3  
Isotope Atom Count: 0  
Rotatable Bond Count: 1  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
Downstream Synthesis Route
99277-23-3    74-86-2   
N'-(vinyloxy)benzenecarboximidamide 

[1]Trofimov;Schmidt;Vasil'Tsov;Mikhaleva;Zaitsev;Morozova;Gorshkov;Henkelmann;Arndt[Synthesis,2001,#16,p.2427-2430]

99277-23-3    1736-55-6 

[1]Trofimov;Schmidt;Vasil'Tsov;Mikhaleva;Zaitsev;Morozova;Gorshkov;Henkelmann;Arndt[Synthesis,2001,#16,p.2427-2430]

Literature fold

Title: Insight into technetium amidoxime complex: oxo technetium(V) complex of N-substituted benzamidoxime as new basic structure for molecular imaging.

Journal: Inorganic chemistry20110207

Title: Reduction of N(ω)-hydroxy-L-arginine by the mitochondrial amidoxime reducing component (mARC).

Journal: The Biochemical journal20110115

Title: A novel and specific fluorescence reaction for uracil.

Journal: Analytica chimica acta20100803

Title: The fourth molybdenum containing enzyme mARC: cloning and involvement in the activation of N-hydroxylated prodrugs.

Journal: Journal of medicinal chemistry20081225

Title: Involvement of stearoyl-CoA desaturase in the reduction of amidoxime prodrugs.

Journal: Xenobiotica; the fate of foreign compounds in biological systems20080901

Title: Identification of the missing component in the mitochondrial benzamidoxime prodrug-converting system as a novel molybdenum enzyme.

Journal: The Journal of biological chemistry20061117

Title: Hepatic, extrahepatic, microsomal, and mitochondrial activation of the N-hydroxylated prodrugs benzamidoxime, guanoxabenz, and Ro 48-3656 ([[1-[(2s)-2-[[4-[(hydroxyamino)iminomethyl]benzoyl]amino]-1-oxopropyl]-4-piperidinyl]oxy]-acetic acid).

Journal: Drug metabolism and disposition: the biological fate of chemicals20051101

Title: Characterization and partial purification of the rat and human enzyme systems active in the reduction of N-hydroxymelagatran and benzamidoxime.

Journal: Drug metabolism and disposition: the biological fate of chemicals20050401

Title: Metabolism of benzamidoxime (N-hydroxyamidine) in human hepatocytes and role of UDP-glucuronosyltransferases.

Journal: Xenobiotica; the fate of foreign compounds in biological systems20050101

Title: Phase 2 metabolites of N-hydroxylated amidines (amidoximes): synthesis, in vitro formation by pig hepatocytes, and mutagenicity testing.

Journal: Chemical research in toxicology20010301

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