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VHR DQ BO1 FO1

Names

[ CAS No. ]:
22080-96-2

[ Name ]:
VHR DQ BO1 FO1

[Synonym ]:
4-Hydroxy-2,6-dimethoxybenzaldehyde
2,5-DIHYDROXY-DL-PHENYLALANINE
2,6-Dimethoxy-4-hydroxybenzaldehyde
4-Hydroxy-2,6-dimethoxy-benzaldehyd
syringaldehyde
MFCD01407645
Benzaldehyde, 4-hydroxy-2,6-dimethoxy-
4-formyl-3,5-dimethoxyphenol
4-hydroxy-2,6-dimethoxy-benzaldehyde
VHR DQ BO1 FO1
3,5-Dimethoxy-4-formylphenol
Ethanal,2-(4-hydroxy-2,6-dimethoxyphenyl)

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
370.4±37.0 °C at 760 mmHg

[ Melting Point ]:
225 °C (dec.)(lit.)

[ Molecular Formula ]:
C9H10O4

[ Molecular Weight ]:
182.173

[ Flash Point ]:
152.7±20.0 °C

[ Exact Mass ]:
182.057907

[ PSA ]:
55.76000

[ LogP ]:
1.66

[ Vapour Pressure ]:
0.0±0.9 mmHg at 25°C

[ Index of Refraction ]:
1.568

[ Storage condition ]:
Keep Cold

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Synthetic Route

Precursor & DownStream

Articles

Liquid-phase combinatorial synthesis of 1,4-benzodiazepine-2,5-diones as the candidates of endothelin receptor antagonism.

J. Comb. Chem. 6(1) , 99-104, (2004)

A library of 1,4-benzodiazepine-2,5-dione dicarboxylate derivatives containing aryl substituents at N(1)- and N(4)-positions to mimic the amino acid residues of Try-13, Phe-14, and Asp-18 in endotheli...

Antibacterial activities of phenolic benzaldehydes and benzoic acids against Campylobacter jejuni, Escherichia coli, Listeria monocytogenes, and Salmonella enterica.

J. Food Prot. 66(10) , 1811-21, (2003)

We evaluated the bactericidal activities of 35 benzaldehydes, 34 benzoic acids, and 1 benzoic acid methyl ester against Campylobacter jejuni, Escherichia coli O157:H7, Listeria monocytogenes, and Salm...

A Structure-Based Activation Model of Phenol-Receptor Protein Interactions. Lee K.

Bull. Korean Chem. Soc. 18 , 16-22, (1997)


More Articles


Related Compounds

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