31656-62-9

Basic information

• Product Name: BENZAMIDE-15N
• Synonyms: BENZAMIDE-15N;BENZAMIDE-15N, 99 ATOM % 15N;BENZAMIDE-15N 98+ ATOM % 15N;Benzamide-15N solution
• CAS NO: 31656-62-9
• Molecular Formula: C₇H₇NO
• Molecular Weight: 122.15
• Product Categories: Alphabetical Listings;B;Stable Isotopes
• Mol File: 31656-62-9.mol
• Article Data: 13

Chemical Properties

• Melting Point: 125-128 °C(lit.)
• Flash Point: 87 °C
• Appearance: /
• Density: 1.12 g/cm³
• Refractive Index: 1.564
• Storage Temp.: Room Temperature
• Solubility: Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
• CAS DataBase Reference: BENZAMIDE-15N(CAS DataBase Reference)
• NIST Chemistry Reference: BENZAMIDE-15N(31656-62-9)
• EPA Substance Registry System: BENZAMIDE-15N(31656-62-9)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• Safety Statements: 36
• WGK Germany: 3
• Hazardous Substances Data: 31656-62-9(Hazardous Substances Data)

Usage

Uses

Benzamide-15N is labelled Benzamide which is a useful synthetic intermediate. Benzamide is a specific inhibitor of poly(ADP-ribose)polymerase. It prevents glutamate- and methamphetamine-induced neurotoxicity in vitro in C57B1/6N mouse.

InChI:InChI=1/C7H7NO/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H2,8,9)/i8+1

Upstream product

• 98-88-4 benzoyl chloride 
• 100-52-7 benzaldehyde 

Downstream Products

• 440345-33-5 thiobenzamide-15N 
• 24949-34-6 <15N>benzonitrile 
• 1421014-75-6 (1S,2S)-15N-2-benzyl-1-phenylpropane-1,2-diamine hydrochloride 
• 1421014-93-8 (1R,2S)-15N₁,N₂,N₂-tribenzyl-1-(4-fluorophenyl)-3-methylbutane-1,2-diamine 
• 1421014-97-2 (1S,2R)-15N₁,N₂,N₂-tribenzyl-1-phenylpropane-1,2-diamine 
• 42927-57-1 15N-benzylamine 
• 7022-92-6 (15N)-aniline 
• 1438854-07-9 1-benzoylpiperidine-¹⁵N 
• 1438854-08-0 1-benzylpiperidine-¹⁵N 
• 1430583-76-8 [¹⁵N]-N-benzyl(trimethylsilyl)amine 
• 1485-70-7 N-benzylbenzamide 
• 1234319-90-4 [1-⁽¹⁵⁾N,2-⁽¹⁵⁾NH₂]-2',3',5'-tri-O-acetyl-2-N-benzoyl-6-O-benzylguanosine 
• 1234319-84-6 [2-⁽¹⁵⁾NH₂]-2',3',5'-tri-O-acetyl-2-N-benzoyl-6-O-benzylguanosine 

Relevant articles and documents

Amine-chelated aryllithium reagents - Structure and dynamics

Multinuclear NMR studies of five-membered-ring amine chelated aryllithium reagents 2-lithio-N,N-dimethylbenzylamine (1), the diethylamine and diisopropylamino analogues (2, 3), and the o-methoxy analogue (4), isotopically enriched in 6Li and s

Structures of silver nitrate complexes with quinolines according to NMR data

Silver(I) nitrate complexes [AgNO3(L)2], where L is quinoline or 2-, 4-, and 8-methylquinoline, are synthesized and studied by the multinuclear NMR (1H, 13C, 15N) method in acetonitrile. The influence

NMR studies on the structure of a lithium amide-chiral diether complex for an asymmetric reaction

The combination of a chiral diether ligand and a lithium benzyl(trimethylsilyl)amide is a powerful lithium amide reagent for asymmetric conjugate amination of enoate in a toluene solvent. The structure of the chiral diether-lithium amide complex in soluti