1208-03-3

Basic information

• Product Name: BENZALDEHYDE NITROGEN MUSTARD
• Synonyms: BENZALDEHYDE NITROGEN MUSTARD;TIMTEC-BB SBB007649;P-N,N-BIS(2-CHLOROETHYL)AMINOBENZALDEHYDE;4-(bis(2-chloroethyl)amino)benzaldehyde;4-(N,N-Bis(2-chloroethyl)amino)benzaldehyde;4-[Bis(-chloroethyl)amino]benzaldehyde;4-Aminobenzaldehyde, N,N-di[2-chloroethyl]-;4-Formyl-N,N-di(2-chloroethyl)benzenamine
• CAS NO: 1208-03-3
• Molecular Formula: C₁₁H₁₃Cl₂NO
• Molecular Weight: 246.13
• Product Categories: Aldehydes;C10 to C21;Carbonyl Compounds
• Mol File: 1208-03-3.mol

Chemical Properties

• Melting Point: 86-90 °C
• Boiling Point: 384.8 °C at 760 mmHg
• Flash Point: 186.5 °C
• Appearance: /
• Density: 1.263 g/cm³
• Vapor Pressure: 3.99E-06mmHg at 25°C
• Refractive Index: 1.595
• PKA: 1.02±0.50(Predicted)
• CAS DataBase Reference: BENZALDEHYDE NITROGEN MUSTARD(CAS DataBase Reference)
• NIST Chemistry Reference: BENZALDEHYDE NITROGEN MUSTARD(1208-03-3)
• EPA Substance Registry System: BENZALDEHYDE NITROGEN MUSTARD(1208-03-3)

Safety Data

• Hazard Codes: C
• Statements: 22-34
• Safety Statements: 26-36/37/39-45
• RIDADR: UN 2923 8/PG 3
• WGK Germany: 3
• RTECS: CU4800000
• Hazardous Substances Data: 1208-03-3(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
BENZALDEHYDE NITROGEN MUSTARD is used as a potential antitumor agent for its ability to damage DNA and inhibit cell proliferation, which can be beneficial in treating cancer.
Used in Cancer Therapy Research:
In cancer therapy research, BENZALDEHYDE NITROGEN MUSTARD is utilized as a subject of study to understand its cytotoxic and mutagenic properties, aiming to develop it into a viable treatment option for various types of cancer.
Used in Toxicology Studies:
Due to its known toxicity to normal cells and potential health risks, BENZALDEHYDE NITROGEN MUSTARD is also used in toxicology studies to assess its safety profile and determine the extent of its harmful effects on biological systems.

InChI:InChI=1/C11H13Cl2NO/c12-5-7-14(8-6-13)11-3-1-10(9-15)2-4-11/h1-4,9H,5-8H2

Upstream product

• 93-61-8 N-methyl-N-phenylformamide 
• 553-27-5 aniline mustard 
• 68-12-2 N,N-dimethyl-formamide 
• 99703-55-6 N,N-diethoxy aniline 
• 37934-06-8 N-phenyldiethanolamine 
• 120-07-0 2,2'-(phenylimino)bis[ethanol] 
• 62-53-3 aniline 

Downstream Products

• 117044-82-3 N,N-bis-(2-chloro-ethyl)-4-[trans-2-(4-methyl-[2]quinolyl)-vinyl]-aniline; hydrochloride 
• 114223-61-9 isonicotinic acid-{4-[bis-(2-chloro-ethyl)-amino]-benzylidenehydrazide} 
• 110175-99-0 2-amino-5-{4-[bis-(2-chloro-ethyl)-amino]-benzylidene}-1H-pyrimidine-4,6-dione 
• 68961-21-7 5-{4-[bis-(2-chloro-ethyl)-amino]-benzylidene}-barbituric acid 
• 49581-03-5 5-{4-[bis-(2-chloro-ethyl)-amino]-benzylidene}-2-thio-barbituric acid 
• 94964-38-2 4-{(Z)-4-[bis-(2-chloro-ethyl)-amino]-benzylidene}-5-methyl-2-phenyl-2,4-dihydro-pyrazol-3-one 
• 5445-69-2 2-phenyl-quinoline-4-carboxylic acid-{4-[bis-(2-chloro-ethyl)-amino]-benzylidenehydrazide} 
• 114225-41-1 7-{4-[bis-(2-chloro-ethyl)-amino]-benzylidene}-2-methyl-3H-thiazolo[2,3-f]purine-4,6-dione 
• 92550-28-2 2-Cyan-5-<4-(N,N-bis-<2-chlorethyl>-amino)-benzylidenamino>-thiazol 
• 93867-36-8 5-{4-[bis-(2-chloro-ethyl)-amino]-benzylideneamino}-thiazole-2-carboxylic acid amide 
• 97283-99-3 5-{4-[bis-(2-chloro-ethyl)-amino]-benzylideneamino}-thiazole-2-carbothioic acid amide 
• 95426-27-0 N-{4-[bis-(2-chloro-ethyl)-amino]-benzylidene}-4-thiazol-2-yl-aniline 
• 95426-28-1 N-{4-[bis-(2-chloro-ethyl)-amino]-benzylidene}-4-thiazol-4-yl-aniline 
• 95426-26-9 {4-[bis-(2-chloro-ethyl)-amino]-benzylidene}-(4-phenyl-thiazol-2-yl)-amine 

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