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
• Article Data: 27

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

General Description

Benzaldehyde nitrogen mustard is a chemical compound that belongs to the class of nitrogen mustard derivatives and contains a benzaldehyde functional group. BENZALDEHYDE NITROGEN MUSTARD has been studied for its potential use as an antitumor agent due to its ability to damage DNA and inhibit cell proliferation. It is known for its cytotoxic and mutagenic properties and has been investigated for its potential use in cancer therapy. However, the compound is also known to be toxic to normal cells and has been associated with potential health risks, so further research is needed to fully understand its potential therapeutic applications.

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 
• 120-07-0 2,2'-(phenylimino)bis[ethanol] 
• 37934-06-8 N-phenyldiethanolamine 
• 62-53-3 aniline 
• 99703-55-6 N,N-diethoxy 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 
• 117881-63-7 2-{4-[bis-(2-chloro-ethyl)-amino]-trans-styryl}-1,4-dimethyl-quinolinium; iodide 
• 112508-76-6 2-{4-[bis-(2-chloro-ethyl)-amino]-phenyl}-quinoline-4-carboxylic acid 
• 103155-77-7 4-amino-benzoic acid-{4-[bis-(2-chloro-ethyl)-amino]-benzylidenehydrazide} 
• 10072-37-4 bis-(2-chloro-ethyl)-(trans-stilbenyl-(4))-amine 
• 1204-86-0 4-(4-morpholinyl)benzaldehyde 
• 27914-17-6 2,2'-(4-formyl-phenylimino)-bis-ethanesulfonic acid 

Relevant articles and documents

Highly sensitive and selective fluorescent chemosensors for Hg(II) in an aqueous environment based on carbamodithioate

Two highly sensitive (detection limits ～20 nM) and selective (selectivity >30) fluorescent chemosensors were developed for detecting Hg2+ in a fully aqueous environment by using the rarely-studied carbamodithioate to create an Hg2+ binding site.

Cation-Selective and Anion-Controlled Fluorogenic Behaviors of a Benzothiazole-Attached Macrocycle That Correlate with Structural Coordination Modes

We report how the metal cation and its counteranions cooperate in the complexation-based macrocyclic chemosensor to monitor the target metal ion via the specific coordination modes. The benzothiazolyl group bearing NO2S2-macrocycle L

Design, synthesis and structural optimization of two click modified butterfly molecules: Aggregation induced ratiometric fluorescence change and ICT associated hydrogen bonding effect in solvatochromic analysis

Two click modified butterfly molecules are designed and synthesized having presence and absence of the aggregative moiety to differ between aggregation induced ratiometric emission changes via excimer formation and ICT associated hydrogen bonding effect.

Imidazole heterocyclic derivative containing mustard and preparation method and application thereof

More specifically, N - phenyldiethanolamine is used as a raw material, Vilsmerier reagents are reacted to obtain a mustard intermediate, and a mustard intermediate and a phenanthrene derivative are used. The preparation method of the phenanthroimidazole d

Nitrogen mustard-containing terpyridyl iron/ruthenium complex, and synthesis method and application thereof

The invention discloses a nitrogen mustard-containing terpyridyl iron/ruthenium complex , a synthesis method and application, and belongs to the technical field of drug synthesis. The terpyridyl iron/ruthenium complex is shown in the following structural