benzocatechol

Modify Date: 2024-01-11 11:39:33

benzocatechol Structure
benzocatechol structure
Common Name benzocatechol
CAS Number 574-00-5 Molecular Weight 160.169
Density 1.3±0.1 g/cm3 Boiling Point 353.9±15.0 °C at 760 mmHg
Molecular Formula C10H8O2 Melting Point 101-103 °C(lit.)
MSDS Chinese USA Flash Point 181.0±15.0 °C
Symbol GHS07
GHS07
Signal Word Warning

 Names

Name naphthalene-1,2-diol
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Boiling Point 353.9±15.0 °C at 760 mmHg
Melting Point 101-103 °C(lit.)
Molecular Formula C10H8O2
Molecular Weight 160.169
Flash Point 181.0±15.0 °C
Exact Mass 160.052429
PSA 40.46000
LogP 2.11
Vapour Pressure 0.0±0.8 mmHg at 25°C
Index of Refraction 1.726

 Safety Information

Symbol GHS07
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
Risk Phrases 36/37/38
Safety Phrases S26-S37/39
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2907299090

 Synthetic Route

 Customs

HS Code 2907299090
Summary 2907299090 polyphenols; phenol-alcohols。supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward)。VAT:17.0%。tax rebate rate:9.0%。MFN tariff:5.5%。general tariff:30.0%

 Articles17

More Articles
Identifying chelators for metalloprotein inhibitors using a fragment-based approach.

J. Med. Chem. 54 , 591-602, (2011)

Fragment-based lead design (FBLD) has been used to identify new metal-binding groups for metalloenzyme inhibitors. When screened at 1 mM, a chelator fragment library (CFL-1.1) of 96 compounds produced...

Selective antiproliferative activity of hydroxynaphthyl-beta-D-xylosides.

J. Med. Chem. 49 , 1932-8, (2006)

The antiproliferative activity of the 14 isomeric monoxylosylated dihydroxynaphthalenes has been tested in vitro toward normal HFL-1 and 3T3 A31 cells as well as transformed T24 and 3T3 SV40 cells. Th...

Metabolism of acenaphthylene via 1,2-dihydroxynaphthalene and catechol by Stenotrophomonas sp. RMSK.

Biodegradation 20(6) , 837-43, (2009)

Stenotrophomonas sp. RMSK capable of degrading acenaphthylene as a sole source of carbon and energy was isolated from coal sample. Metabolites produced were analyzed and characterized by TLC, HPLC and...

 Synonyms

1,2-Naphthalenediol
benzocatechol
Naphthalene-1,2-diol
MFCD00003959
EINECS 209-365-2
1,2-Dihydroxynaphthalene
dihydroxynaphthalene
naphthalenediol
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