Methyl 3,5-dihydroxybenzoate

Names

[ Name ]:
Methyl 3,5-dihydroxybenzoate

[Synonym ]:
3,5-dihydroxy methyl benzoate
3,5-dihydroxybenzoic acid methyl ester
methyl 3,5-dihydroxy-benzoate
Benzoic acid, 3,5-dihydroxy-, methyl ester
α-Resorcylic Acid Methyl Ester
Methyl-3,5-dihydroxybenzolcarboxylat
1-carbomethoxy-3,5-dihydroxybenzene
Methyl 3,5-dihydroxybenzoate
Benzoic acid,3,5-dihydroxy-,methyl ester
MFCD00002289
EINECS 218-426-2

Biological Activity

[Description]:

Methyl 3,5-dihydroxybenzoate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

[In Vitro]

Methyl 3,5-dihydroxybenzoate 用于核树枝状聚合物的合成。

Chemical & Physical Properties

[ Density]:
1.4±0.1 g/cm3

[ Boiling Point ]:
349.4±12.0 °C at 760 mmHg

[ Melting Point ]:
167-170 °C(lit.)

[ Molecular Formula ]:
C₈H₈O₄

[ Molecular Weight ]:
168.15

[ Flash Point ]:
147.6±13.1 °C

[ Exact Mass ]:
168.042252

[ PSA ]:
66.76000

[ LogP ]:
1.60

[ Vapour Pressure ]:
0.0±0.8 mmHg at 25°C

[ Index of Refraction ]:
1.588

MSDS

Click to get detail 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-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2918290000

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2918290000

[ Summary ]:
HS: 2918290000 other carboxylic acids with phenol function but without other oxygen function, their anhydrides, halides, peroxides, peroxyacids and their derivatives Tax rebate rate:9.0% Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward) VAT:17.0% MFN tariff:6.5% General tariff:30.0%

Articles

New ribonucleotide reductase inhibitors with antineoplastic activity.

Cancer Res. 39(3) , 844-51, (1979)

Synthesis of cored dendrimers. Wendland MS and Zimmerman SC.

J. Am. Chem. Soc. 121(6) , 1389-90, (1999)

Macrocyclic polymers. 1. Synthesis of a poly (ester crown) based on bis (5-carboxy-1, 3-phenylene)-32-crown-10 and 4, 4'-isopropylidenediphenol (bisphenol A). Delaviz Y and Gibson HW.

Macromolecules 25(1) , 18-20, (1992)