3,5-Dimethylbenzaldehyde

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Names

[ CAS No. ]:
5779-95-3

[ Name ]:
3,5-Dimethylbenzaldehyde

[Synonym ]:
MFCD00082777
Benzaldehyde, 3,5-dimethyl-
3,5-dimethylbenzaledehyde
3,5-Dimethyl-benzaldehyde
VHR C1 E1
m-Xylene-5-carboxaldehyde
3,5-Dimethylbenzaldehyde
Benzaldehyde,3,5-dimethyl
3,5-dimethylphenylaldehyde
3,5-Dimethyl-benzaldehyd

Chemical & Physical Properties

[ Density]:
1.0±0.1 g/cm3

[ Boiling Point ]:
221.0±0.0 °C at 760 mmHg

[ Melting Point ]:
8-10 °C

[ Molecular Formula ]:
C9H10O

[ Molecular Weight ]:
134.175

[ Flash Point ]:
87.5±5.0 °C

[ Exact Mass ]:
134.073166

[ PSA ]:
17.07000

[ LogP ]:
2.56

[ Vapour Pressure ]:
0.1±0.4 mmHg at 25°C

[ Index of Refraction ]:
1.551

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves

[ Hazard Codes ]:
Xn:Harmful;

[ Risk Phrases ]:
R22

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2912299000

Precursor & DownStream

Precursor

  • carbon monoxide
  • 1-Iodo-3,5-dimethylbenzene
  • 1-Bromo-3,5-dimethylbenzene
  • a-Bromomesitylene
  • Mesitylene
  • 3,5-dimethylbenzyl alcohol
  • N,N-Dimethylformamide
  • 3,5-Dimethylbenzoic acid
  • chloromesitylene
  • Acetone cyanohydrin

DownStream

  • 3,5-Dimethylbenzoic acid
  • 3,5-dimethylbenzyl alcohol
  • Mesitylene
  • 1-(3,5-Dimethylphenyl)methanamine
  • 5,7-Dimethyl-1-indanone
  • 3,5-Dimethylbenzoyl chloride
  • Methyl 3,5-dimethylbenzoate
  • 2,5,7-Trimethyl-1-indanone
  • 2-[(3,5-dimethylphenyl)methyl]-1,3,5-trimethylbenzene
  • 3,5-DIMETHYLBENZALDEHYDE OXIME

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

Synthesis and antiviral activity of 6-benzyl analogs of 1-[(2-hydroxyethoxy)methyl]-6-(phenylthio)thymine (HEPT) as potent and selective anti-HIV-1 agents.

J. Med. Chem. 38(15) , 2860-5, (1995)

Several 6-benzyl analogs of 1-[(2-hydroxyethoxy)methyl]-6-(phenylthio)thymine (1; HEPT) were synthesized and evaluated for their anti-HIV-1 activity. LDA (lithium diisopropylamide) lithiation of 5-eth...

A new substrate for the Biginelli cyclocondensation: direct preparation of 5-unsubstituted 3,4-dihydropyrimidin-2(1H)-ones from a beta-keto carboxylic acid

J. Org. Chem. 65(20) , 6777-9, (2000)

Design and synthesis of novel chiral pyrrolidine-based diamines with C2-symmetry. Nakajima M, et al.

Tetrahedron 49(43) , 9735-9750, (1993)


More Articles


Related Compounds

  • 3,5-DIMETHYLBENZALDEHYDE OXIME
  • 4-Bromo-3,5-dimethylbenzaldehyde
  • 4-amino-3,5-dimethylbenzaldehyde
  • 2-amino-3,5-dimethylbenzaldehyde
  • 2-bromo-3,5-dimethylbenzaldehyde
  • 4-Nitro-3,5-dimethylbenzaldehyde