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Structure

3-Methoxybenzylamine

CAS
5071-96-5
Catalog Number
ACM5071965
Category
Other Products
Molecular Weight
137.18
Molecular Formula
C8H11NO

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Specification

Synonyms
RARECHEM AL BW 0160;M-METHOXYBENZYLAMINE;(3-Methoxyphenyl)methanamine;3-methoxy-benzenemethanamin;Benzenemethanamine, 3-methoxy-;Benzylamine, m-methoxy-;m-methoxy-benzylamin;3-METHOXYBENZYLAMINE
Boiling Point
140°C37mm Hg(lit.)
Flash Point
>230°F
Density
1.072g/mL at 25°C(lit.)
Hazard Statements
Xi,C,Xn
Safety Description
26-36-45-36/37/39
Supplemental Hazard Statements
H318-H302-H315-H319-H335-H314
Symbol
GHS07,GHS05
What is the molecular formula of 3-Methoxybenzylamine?

The molecular formula of 3-Methoxybenzylamine is C8H11NO.

What is the molecular weight of 3-Methoxybenzylamine?

The molecular weight of 3-Methoxybenzylamine is 137.18 g/mol.

What are some synonyms for 3-Methoxybenzylamine?

Some synonyms for 3-Methoxybenzylamine are 3-Methoxybenzylamine, m-Methoxybenzylamine, and (3-Methoxyphenyl)methanamine.

When was the PubChem CID for 3-Methoxybenzylamine created?

The PubChem CID for 3-Methoxybenzylamine was created on March 26, 2005.

What is the InChIKey for 3-Methoxybenzylamine?

The InChIKey for 3-Methoxybenzylamine is GRRIMVWABNHKBX-UHFFFAOYSA-N.

What is the XLogP3 value for 3-Methoxybenzylamine?

The XLogP3 value for 3-Methoxybenzylamine is 0.9.

How many hydrogen bond donor counts does 3-Methoxybenzylamine have?

3-Methoxybenzylamine has 1 hydrogen bond donor count.

How many hydrogen bond acceptor counts does 3-Methoxybenzylamine have?

3-Methoxybenzylamine has 2 hydrogen bond acceptor counts.

What is the topological polar surface area of 3-Methoxybenzylamine?

The topological polar surface area of 3-Methoxybenzylamine is 35.2 Å2.

Is 3-Methoxybenzylamine a covalently-bonded unit?

Yes, 3-Methoxybenzylamine is a covalently-bonded unit.

Upstream Synthesis Route 1

  • 38489-80-4
  • 5071-96-5

Reference: [1] Journal of the Chemical Society, 1932, p. 696,703
[2] Science China Chemistry, 2012, vol. 55, # 3, p. 435 - 442
[3] Synthetic Communications, 2013, vol. 43, # 16, p. 2127 - 2133
[4] European Journal of Medicinal Chemistry, 2017, vol. 135, p. 24 - 33

Upstream Synthesis Route 2

  • 1527-89-5
  • 5071-96-5

Reference: [1] Angewandte Chemie - International Edition, 2016, vol. 55, # 47, p. 14653 - 14657

Upstream Synthesis Route 3

  • 153903-22-1
  • 5071-96-5

Reference: [1] Tetrahedron Letters, 2000, vol. 41, # 36, p. 7013 - 7016

Upstream Synthesis Route 4

  • 5813-86-5
  • 5071-96-5

Reference: [1]Journal of the American Chemical Society,1955,vol. 77,p. 109,112
Org. Synth. Coll.,1963,vol. Vol. IV,p. 780,782
[2]Chemical Communications,2014,vol. 50,p. 9349 - 9352

Downstream Synthesis Route 1

  • 5071-96-5
  • 85952-30-3
  • 111874-86-3

Reference: [1]Orazi, Orfeo O.; Corral, Renee A.; Giaccio, Hector
[Journal of the Chemical Society. Perkin transactions I, 1986, p. 1977 - 1982]

* For details of the synthesis route, please refer to the original source to ensure accuracy.

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