4-Methyl-1-naphthaldehyde

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Names

[ CAS No. ]:
33738-48-6

[ Name ]:
4-Methyl-1-naphthaldehyde

[Synonym ]:
4-Methyl-1-naphthaldehyde
MFCD00060691
1-Naphthalenecarboxaldehyde, 4-methyl-
4-methylnaphthalene-1-carbaldehyde

Chemical & Physical Properties

[ Density]:
1.1±0.1 g/cm3

[ Boiling Point ]:
318.0±11.0 °C at 760 mmHg

[ Melting Point ]:
32-36 °C(lit.)

[ Molecular Formula ]:
C12H10O

[ Molecular Weight ]:
170.207

[ Flash Point ]:
186.5±5.5 °C

[ Exact Mass ]:
170.073166

[ PSA ]:
17.07000

[ LogP ]:
3.33

[ Vapour Pressure ]:
0.0±0.7 mmHg at 25°C

[ Index of Refraction ]:
1.656

[ Storage condition ]:
2-8°C

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36/37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2912299000

Precursor & DownStream

Precursor

  • carbon monoxide
  • 1-Methylnaphthalene
  • 1,4-Dimethylnaphthalene
  • acetic acid
  • N,N-DIFORMYLFORMAMIDE
  • formyl fluoride
  • Malonic acid
  • (4-Methyl-1-naphthyl)methanol
  • HYDROGEN CYANIDE
  • Dichloromethyl methyl ether

DownStream

  • 4-Methyl-1-naphthoic acid
  • 4-Methyl-1-naphthol

Customs

[ HS Code ]: 2912299000

[ Summary ]:
2912299000. other cyclic aldehydes without other oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0%

Articles

5-Substituted [1]pyrindine derivatives with antiproliferative activity.

Eur. J. Med. Chem. 45 , 896-901, (2010)

We report herein the synthesis of 5-substituted [1]pyrindine derivatives and the evaluation of their antiproliferative properties on HeLa cells, a cervical carcinoma tumor cell line, and on the melano...

Synthesis and tumor-initiating activities of dimethylchrysenes.

Chem. Res. Toxicol. 1(6) , 349-55, (1988)

Previous studies have shown that 5-methylchrysene (5-MeC) is more carcinogenic on mouse skin than the other methylchrysenes and that the structural requirements favoring tumorigenicity of methylated p...

The influence of aromatic compound protonation on the regioselectivity of Gattermann-Koch formylation. Tanaka M, et al.

Chem. Commun. (Camb.) 2 , 159-160, (1996)


More Articles

Related Compounds

  • 7,8-Dihydroxy-6-(2-hydroxy-2-propanyl)-4-methyl-1-naphthaldehyde
  • 2-[[4-methyl-3-(1-prop-2-enoyloxypropan-2-yloxycarbonylamino)phenyl]carbamoyloxy]propyl prop-2-enoate
  • 4-methyl-1-(6-methylhept-5-en-2-yl)bicyclo[3.1.0]hexan-4-ol
  • 4-methyl-1-phenoxypent-3-en-2-one
  • 4-Methyl-1-(trimethylsiloxy)-3,4-dihydronaphthalin
  • 4-methyl-1-propan-2-yldibenzofuran