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Details

Stereochemistry ACHIRAL
Molecular Formula C6H5.Na
Molecular Weight 100.0937
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PHENYLSODIUM

SMILES

[Na+].C1=CC=[C-]C=C1

InChI

InChIKey=KSMWLICLECSXMI-UHFFFAOYSA-N
InChI=1S/C6H5.Na/c1-2-4-6-5-3-1;/h1-5H;/q-1;+1

HIDE SMILES / InChI

Molecular Formula Na
Molecular Weight 22.9898
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C6H6
Molecular Weight 78.1118
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Phenyl sodium is organometallic compound. It is used to carry exchange reactions to produce phenylmalonic acid.

Originator

Curator's Comment: Am. Chem. Journal, 29, 589 (1903).

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Modifications in the metabolic pathways of benzene in streptozotocin-induced diabetic rat.
1999 Aug
Formation and inhibition of chloroaromatic micropollutants formed in incineration processes.
2001 Apr
Photocleavage of DNA by 4'-bromoacetophenone analogs.
2001 Feb
Sensitive and rapid method for the simultaneous quantification of the HIV-protease inhibitors indinavir, nelfinavir, ritonavir, and saquinavir in human plasma by reversed-phase liquid chromatography.
2001 Feb
Urinary benzene as a biomarker of exposure among occupationally exposed and unexposed subjects.
2001 Feb
BAPS prize-1999: Lung growth induced by prenatal tracheal occlusion and its modifying factors: a study in the rat model of congenital diaphragmatic hernia.
2001 Feb
The role of the hinge region of the luteinizing hormone receptor in hormone interaction and signal generation.
2001 Feb 2
Enhancement, relaxation, and reversal of the stereoselectivity for phosphotriesterase by rational evolution of active site residues.
2001 Feb 6
Combining membrane extraction with mobile gas chromatography for the field analysis of volatile organic compounds in contaminated waters.
2001 Feb 9
BTEX catabolism interactions in a toluene-acclimatized biofilter.
2001 Jan
[[Physical chemical, pharmacological and toxicologic properties of fomocaine metabolites] ].
2001 Jan
Interfacial study of benzenesulfinate chemisorbed on silver.
2001 Jan
Determination of low concentrations of benzene in urine using multi-dimensional gas chromatography.
2001 Jan
Electric field-induced mobilisation of multiphase solution systems based on the nitration of benzene in a micro reactor.
2001 Jan
Triarylpyrazoles with basic side chains: development of pyrazole-based estrogen receptor antagonists.
2001 Jan
Two 1-substituted 4-nitroimidazoles.
2001 Jan
A saccharinate-iron(II) complex with a free saccharin molecule present, [Fe(phen)3]sac2.sacH.6H2O.
2001 Jan
Photoinduced ortho [2 + 2] cycloaddition of double bonds to triplet benzenes.
2001 Jan
Proximal cysteine residue is essential for the enzymatic activities of cytochrome P450cam.
2001 Jan
Benzene in the environment: an assessment of the potential risks to the health of the population.
2001 Jan
Butachlor, thiobencarb, and chlomethoxyfen movement in subtropical soils.
2001 Jan
Antagonists of the human CCR5 receptor as anti-HIV-1 agents. Part 2: structure-activity relationships for substituted 2-Aryl-1-[N-(methyl)-N-(phenylsulfonyl)amino]-4-(piperidin-1-yl)butanes.
2001 Jan 22
Design and synthesis of sialyl Lewis x mimics as E-selectin inhibitors.
2001 Jan 22
Effects of mono-, di- and tri-hydroxybenzoic acids on the nitrosation of propranolol: structure-activity relationship.
2001 Jan 25
The influence of GSTM1 null genotype on susceptibility to in vitro oxidative stress.
2001 Jan 26
The influence of different soil constituents on the reaction kinetics of wet oxidation of the creosote compound quinoline.
2001 Jan 29
Benzene-induced myelodysplastic syndrome.
2001 Jan-Feb
A rigid linker-scaffold for solid-phase synthesis of dimeric pharmacophores.
2001 Jan-Feb
Oxidation of polychlorinated benzenes by genetically engineered CYP101 (cytochrome P450(cam)).
2001 Mar
Exposure to benzene in urban workers: environmental and biological monitoring of traffic police in Rome.
2001 Mar
Predicted Michaelis-Menten complexes of cocaine-butyrylcholinesterase. Engineering effective butyrylcholinesterase mutants for cocaine detoxication.
2001 Mar 23
Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Sat Dec 16 07:56:19 GMT 2023
Edited
by admin
on Sat Dec 16 07:56:19 GMT 2023
Record UNII
SNA8TW8V4T
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PHENYLSODIUM
Systematic Name English
SODIUM, PHENYL-
Systematic Name English
BENZENE SODIUM SALT [MI]
Common Name English
SODIOBENZENE
Systematic Name English
Code System Code Type Description
FDA UNII
SNA8TW8V4T
Created by admin on Sat Dec 16 07:56:19 GMT 2023 , Edited by admin on Sat Dec 16 07:56:19 GMT 2023
PRIMARY
MERCK INDEX
m2338
Created by admin on Sat Dec 16 07:56:19 GMT 2023 , Edited by admin on Sat Dec 16 07:56:19 GMT 2023
PRIMARY Merck Index
WIKIPEDIA
Phenylsodium
Created by admin on Sat Dec 16 07:56:19 GMT 2023 , Edited by admin on Sat Dec 16 07:56:19 GMT 2023
PRIMARY
PUBCHEM
11007827
Created by admin on Sat Dec 16 07:56:19 GMT 2023 , Edited by admin on Sat Dec 16 07:56:19 GMT 2023
PRIMARY
EPA CompTox
DTXSID301316871
Created by admin on Sat Dec 16 07:56:19 GMT 2023 , Edited by admin on Sat Dec 16 07:56:19 GMT 2023
PRIMARY
CAS
1623-99-0
Created by admin on Sat Dec 16 07:56:19 GMT 2023 , Edited by admin on Sat Dec 16 07:56:19 GMT 2023
PRIMARY