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Molecule
ID:34349
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General Information
Structure
Molecular Formula
C₉H₁₃NO₂
Molecular Mass
167.20502
Exact Mass
167.09462866
Charge
0
InChI
InChI=1S/C9H13NO2/c1-11-8-4-3-7(6-10)9(5-8)12-2/h3-5H,6,10H2,1-2H3
InChIKey
QOWBXWFYRXSBAS-UHFFFAOYSA-N
Canonic Smiles
COc1cc(OC)ccc1CN
Isomeric Smiles
c1cc(c(cc1OC)OC)CN
Calculated Properties
JChem
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
-2.1100907
LogD (pH = 7.4)
-0.7687591
Log P
0.78367174
Molar Refractivity
47.4578
Polarizability
18.725096
Polar Surface Area
44.48
Rotatable Bonds
3
Lipinski's Rule of Five
true
Data Source
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Names and Identifiers
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Registration numbers
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Properties
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Related Proteins
No Data Available
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Molecular Spectra
No Data Available
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Molecule Details
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References
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Bioactivity
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General Information
Calculated Properties
•
RDKit
•
JChem
Data Source
•
Commercial Catalog
•
Academic Data
Names and Identifiers
•
IUPAC name
•
Synonyms
•
IUPAC Traditional name
Registration numbers
•
MDL Number
•
CAS Number
•
PubChem SID
•
PubChem CID
Properties
•
Product Information
•
Safety Information
•
Physical Property
Related Proteins
Molecular Spectra
Molecule Details
•
Sigma Aldrich
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
037102
Sigma Aldrich
432725
Chemik
CHB58034
Enamine
EN300-34182
Bide Pharmatech
BD216141
Alfa Aesar
H27140
A&J Pharmtech
AJA-O4292
Academic Data
PubChem
597250
Names and Identifiers
IUPAC name
(2,4-dimethoxyphenyl)methanamine
Synonyms
1-(2,4-Dimethoxyphenyl)methanamine
2,4-Dimethoxybenzylamine
2,4-二甲氧基苄胺
2,4-Dimethoxybenzylamine
(2,4-dimethoxyphenyl)methanamine
IUPAC Traditional name
(2,4-dimethoxyphenyl)methanamine
Registration numbers
MDL Number
MFCD00052393
CAS Number
20781-20-8
PubChem SID
160997656
24867094
PubChem CID
597250
Properties
Product Information
Purity
95+%
Source
98%
Source
95%
Source
96%
Source
Linear Formula
(CH3O)2C6H3CH2NH2
Source
Safety Information
MSDS Link
Download link
来源
Download link
Source
Storage Warning
IRRITANT
Source
Air Sensitive
Source
TSCA Listed
false
Source
否
Source
Personal Protective Equipment
Faceshields, full-face respirator (US), Gloves, Goggles, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
Source
RID/ADR
UN 2735 8/PG 3
Source
Safety Statements
26
-
27
-
36/37/39
-
45
Source
26
-
36/37/39
-
45
Source
Hazard Class
8
Source
GHS Signal Word
Danger
Source
Risk Statements
34
Source
GHS Precautionary statements
P280
-
P305+P351+P338
-
P310
Source
P260
-
P303+P361+P353
-
P305+P351+P338
-
P301+P330+P331
-
P405
-P501A
Source
German water hazard class
3
Source
GHS Pictograms
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
Source
European Hazard Symbols
Corrosive (C)
Source
GHS Hazard statements
H314
Source
H314
-
H318
Source
UN Number
2735
Source
UN2735
Source
Packing Group
3
Source
III
Source
Physical Property
Refractive Index
n20/D 1.549(lit.)
Source
1.5490
Source
Density
1.113 g/mL at 25 °C(lit.)
Source
1.113
Source
Boiling Point
140 °C/1 mmHg(lit.)
Source
140°C/1mm
Source
Flash Point
113 °C
Source
235.4 °F
Source
>110°C(230°F)
Source
Melting Point
188 - 190°C
Source
Hydrophobicity(logP)
1.102
Source
Molecule Details
Sigma Aldrich
432725
Application
Amine nucleophile used in a study of the 1,4- reactivity of 5-bromo-2-indene-1-one.1
Used to synthesize anti-HIV-1 agents.
Packaging
5, 25 mL in glass bottle
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay