4-Nitrobenzaldehyde

4-Nitrobenzaldehyde Basic information

Product Name:	4-Nitrobenzaldehyde
Synonyms:	4-NITROBENZALDEHYDE;AKOS BBS-00003206;4-nitro-benzaldehyd;Benzaldehyde, p-nitro-;Benzaldehyde,4-nitro-;Benzaldehyde,p-nitro-;p-nitro-benzaldehyd;p-Nitrobenzaldehyde 4-Nitrobenzaldehyde
CAS:	555-16-8
MF:	C7H5NO3
MW:	151.12
EINECS:	209-084-5
Product Categories:	Dyestuff Intermediates;Building Blocks;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks;FINE Chemical & INTERMEDIATES;Aromatic Aldehydes & Derivatives (substituted);Benzaldehyde;Aldehydes;C7;Carbonyl Compounds;Spectroscopy;UV/Vis Reagents;UV/Visible (UV/VIS) Spectroscopy;555-16-8
Mol File:	555-16-8.mol

4-Nitrobenzaldehyde Chemical Properties

Melting point	103-106 °C(lit.)
Boiling point	273.1°C (rough estimate)
density	1,496 g/cm³
refractive index	1.5800 (estimate)
storage temp.	Store below +30°C.
solubility	2.34g/l
form	Crystalline Powder
color	Yellow to brown
Odor	Odorless
Water Solubility	Soluble in water, ethanol, benzene, glacial acetic acid. Slightly soluble in ether.
Sensitive	Air Sensitive
Merck	14,6587
BRN	386796
CAS DataBase Reference	555-16-8(CAS DataBase Reference)
NIST Chemistry Reference	Benzaldehyde, 4-nitro-(555-16-8)
EPA Substance Registry System	Benzaldehyde, 4-nitro- (555-16-8)

Safety Information

Hazard Codes	Xi
Risk Statements	36-43-52/53-36/37/38-68
Safety Statements	26-36/37-61-24/25-36/37/39-36
WGK Germany	2
RTECS	CU7350000
Hazard Note	Irritant
TSCA	Yes
HS Code	29130000
Toxicity	LD50 orally in Rabbit: 4700 mg/kg LD50 dermal Rat 16000 mg/kg

MSDS Information

Provider	Language
4-Nitrobenzaldehyde	English
SigmaAldrich	English
ACROS	English
ALFA	English

4-Nitrobenzaldehyde Usage And Synthesis

Chemical Properties	YELLOW TO BROWN CRYSTALLINE POWDER
Uses	4-Nitrobenzaldehyde was used in the preparation of homoallylic alcohols. It was also used to develop and evaluate a series of tripeptide organocatalysts.
Uses	4-Nitrobenzaldehyde is a benzaldehyde with a nitro group in the para position. It is used as a reagent in decarboxylative aldol reactions that are catalyzed by lipases and proteases in organic co-solvent mixtures.
Definition	ChEBI: 4-nitrobenzaldehyde is a C-nitro compound that is benzaldehyde substituted at the para-position with a nitro group. It is a C-nitro compound and a member of benzaldehydes.
Synthesis Reference(s)	Journal of the American Chemical Society, 78, p. 252, 1956 DOI: 10.1021/ja01582a072 Tetrahedron Letters, 28, p. 4285, 1987 DOI: 10.1016/S0040-4039(00)96486-4
Purification Methods	Purify it as for m-nitrobenzaldehyde above. [Beilstein 7 IV 589.]

4-Nitrobenzaldehyde Preparation Products And Raw materials

Raw materials

Nitric acid-->Government regulation-->4-Nitrotoluene

Preparation Products

Chloramphenicol-->4-NITROSTYRENE-->3-(4-Nitrophenyl)propanoic acid-->3-(4-NITRO-PHENYL)-PROPAN-1-OL-->4-(4-NITROPHENYL)-3-BUTEN-2-ONE-->BODIPY-->1,4-Benzenediamine, N,N-dimethyl-N'-[(4-nitrophenyl)methylene]--->4-FLUORO-4'-NITROBENZOPHENONE-->P-NITROPHENYL PHOSPHATE-->5,15-Di(4-aminophenyl)-10,20-diphenyl porphine-->2-(2-AMINOPHENYL)BENZOTHIAZOLE 97-->N-CAPRIC ACID N-DECYL ESTER-->4-HYDROXY-B-NITROSTYRENE-->4-ACETAMIDOBENZYL ALCOHOL-->4'-(4-AMINOPHENYL)-2,2':6',2''-TERPYRIDINE-->5-(4-NITRO-PHENYL)-2H-TETRAZOLE-->4-NITROCINNAMALDEHYDE

4-chloro-2-nitrobenzaldehyde*crystalline 4-BROMO-3-HYDROXYBENZOIC ACID 3-NITRO BENZALDEHYDE P-NITROBENZOYL-L-GLUTAMIC ACID 4,5-bis(hexyloxy)-2-nitrobenzaldehyde 4-Nitrobenzeneethanol 3-nitrofluoren-9-one 2-NITROBENZALDOXIME, (2-NITROBENZALDEHYDE OXIME) 2-CHLORO-3,4-DIMETHOXY-6-NITROBENZALDEHYDE, TECH ρ-Nitrobenzenesulphonic acid M-NITROBENZALDEHYDE DIMETHYL ACETAL 4-Nitrophthalhydrazide 5-METHOXY-2-NITROBENZALDEHYDE 4-ETHOXY-3-NITROBENZALDEHYDE 97 2-acetamido-3-nitro-9-fluorenone 5-Chloro-2-Nitrobenzaldehyde 2-Nitro-5-Chlorobenzaldehyde N-(4-NITROBENZOYL)-L-GLUTAMIC ACID DIETHYL ESTER 4-NITROBENZALDOXIME, (4-NITROBENZALDEHYDE OXIME)

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