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1,3-Dimethoxybenzene

Names

[ CAS No. ]:
151-10-0

[ Name ]:
1,3-Dimethoxybenzene

[Synonym ]:
dimethyl resorcinol
FEMA 2385
Dimethylresorcinol,Resorcinol dimethyl ether
M-METHOXYANISOLE
Resorcinol Dimethyl Ether
EINECS 205-783-4
m-dimethoxy-benzen
3-METHOXYANISOLE
1,3-Dimethoxybenzene
2,4-dimethoxy-benzene
meta-dimethoxybenzene
M-DIMETHOXYBENZENE
MFCD00008384
2,6-dimethoxybenzene
1,3-methoxybenzenel
Benzene, 1,3-dimethoxy-
1,3-Dimethoxybenzol
1,3-dimethoxy benzene
Resorcin-dimethylether
3-DiMethoxybenzene
Dimethylresorinol
m-Dimethoxy benzene

Biological Activity

[Description]:

1,3-Dimethoxybenzene belongs to the class of organic compounds known as dimethoxybenzenes. 1,3-Dimethoxybenzene is an intermediate in synthesis of organic compounds[1].

[Related Catalog]:

Research Areas >> Others
Signaling Pathways >> Others >> Others

[References]

[1]. Gregory Michael Shutske, et al. Process for the preparation of 2-chloro-1,3-dimethoxybenzene. EP0067342A1

Chemical & Physical Properties

[ Density]:
1.0±0.1 g/cm3

[ Boiling Point ]:
217.5±0.0 °C at 760 mmHg

[ Melting Point ]:
-52°C

[ Molecular Formula ]:
C8H10O2

[ Molecular Weight ]:
138.164

[ Flash Point ]:
87.8±0.0 °C

[ Exact Mass ]:
138.068085

[ PSA ]:
18.46000

[ LogP ]:
1.93

[ Vapour Pressure ]:
0.2±0.4 mmHg at 25°C

[ Index of Refraction ]:
1.488

MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
CZ6474000
CHEMICAL NAME :
Benzene, m-dimethoxy-
CAS REGISTRY NUMBER :
151-10-0
LAST UPDATED :
199701
DATA ITEMS CITED :
3
MOLECULAR FORMULA :
C8-H10-O2
MOLECULAR WEIGHT :
138.18
WISWESSER LINE NOTATION :
1OR CO1

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
900 mg/kg
TOXIC EFFECTS :
Behavioral - somnolence (general depressed activity) Behavioral - tremor Behavioral - ataxia
REFERENCE :
JAPMA8 Journal of the American Pharmaceutical Association, Scientific Edition. (Washington, DC) V.29-49, 1940-60. For publisher information, see JPMSAE. Volume(issue)/page/year: 46,185,1957 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOES - National Occupational Exposure Survey (1983) NOES Hazard Code - X2614 No. of Facilities: 19 (estimated) No. of Industries: 1 No. of Occupations: 1 No. of Employees: 93 (estimated) No. of Female Employees: 56 (estimated)

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;half-mask respirator (US);multi-purpose combination respirator cartridge (US)

[ Hazard Codes ]:
Xi:Irritant

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
NA 1993 / PGIII

[ WGK Germany ]:
2

[ RTECS ]:
CZ6474000

[ HS Code ]:
2909309090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2909309090

[ Summary ]:
2909309090 other aromatic ethers and their halogenated, sulphonated, nitrated or nitrosated derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

Articles

Rotamers of o- and m-dimethoxybenzenes studied by mass-analyzed threshold ionization spectroscopy and theoretical calculations.

J. Phys. Chem. A 114(42) , 11144-52, (2010)

We applied two-color resonant two-photon mass-analyzed threshold ionization (MATI) spectroscopy to investigate the molecular properties of the selected rotamers of o-dimethoxybenzene (ODMB) and m-dime...

Stereoselective glycosylations using oxathiane spiroketal glycosyl donors.

Carbohydr. Res. 348 , 6-13, (2012)

Novel oxathiane spiroketal donors have been synthesised and activated via an umpolung S-arylation strategy using 1,3,5-trimethoxybenzene and 1,3-dimethoxybenzene. The comparative reactivity of the res...

Solvation of dichlorocarbene: complexation with aryl ethers.

J. Phys. Chem. A 114(1) , 209-17, (2010)

Dichlorocarbene (CCl(2)), generated by laser flash photolysis of dichlorodiazirine, formed pi- and O-ylidic complexes with aromatic ethers such as anisole, 1,3-dimethoxybenzene, 1,3,5-trimethoxybenzen...


More Articles


Related Compounds