3,5-Dimethylbenzaldehyde

Names

[ 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

Biological Activity

[Description]:

3,5-Dimethylbenzaldehyde is a building block in the chemical synthesis[1].

[Related Catalog]:

Research Areas >> Others

[References]

[1]. M Tudorie, et al. Coupled large amplitude motions: a case study of the dimethylbenzaldehyde isomers. J Phys Chem A. 2013 Dec 19;117(50):13636-47.

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

Click to get detail 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

DownStream

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)