3-Amino-3-(4-pyridyl)-1-propanol - CAS 865074-65-3

Name: 3-Amino-3-(4-pyridyl)-1-propanol
Brand: BOC Sciences
Rating: 5 (1 reviews)

Catalog:	BB037964
Product Name:	3-Amino-3-(4-pyridyl)-1-propanol
CAS:	865074-65-3
Synonyms:	3-amino-3-pyridin-4-yl-1-propanol; 3-amino-3-pyridin-4-ylpropan-1-ol

Technical Data

Patents

Computed Properties

IUPAC Name:	3-amino-3-pyridin-4-ylpropan-1-ol
Description:	3-Amino-3-(4-pyridyl)-1-propanol (CAS# 865074-65-3 ) is a useful research chemical.
Molecular Weight:	152.19
Molecular Formula:	C8H12N2O
Canonical SMILES:	C1=CN=CC=C1C(CCO)N
InChI:	InChI=1S/C8H12N2O/c9-8(3-6-11)7-1-4-10-5-2-7/h1-2,4-5,8,11H,3,6,9H2
InChI Key:	OPSDHGDMFGAHPA-UHFFFAOYSA-N
LogP:	1.16410

Related Products

Online Inquiry

Name:

* Phone:

* Service & Products of Interested:

Project Description:

* Quantity:

* Email:

* Verification Code:

Customer Support

If the product you need is not in our catalog, please contact us in time to submit your needs. You can help our website get better and better. Why not submit the request today?

Submit Requirement

Customer Centered

Global Delivery

Warehouses in multiple cities to ensure fast delivery

Quality Assurance

Strict process parameter control to ensure product quality

Large Stock

> 20,000 building blocks and intermediates from stock

Process Scale-up

Process scale-up from lab to industrial scale

Flexible Batch Size

Flexible batch size for diverse industrial demands

Related Functional Groups

Alcohols and Derivatives

[113724-48-4]C9H12O2
(R)-1-(2-Methoxyphenyl)ethanol
[62972-93-4]C18H36O
(Z)-11-Octadecen-1-ol
[1946823-77-3]C7H9F3N2O
[1,4-Dimethyl-3-(trifluoromethyl)-1H-pyrazol-5-yl]methanol
[1448610-48-7]C11H13BrO
1-(4-Bromo-3-methylphenyl)cyclobutanol
[1017184-54-1]C9H14N2O
3-Amino-2-(2-pyridylmethyl)-1-propanol
[340774-59-6]C8H8O3S
3-Hydroxy-2,3-dihydrobenzothiophene 1,1-Dioxide

Publication Number	Title	Priority Date
EP-1694630-A1	Improved method for producing chiral or enantiomer-enriched beta-amino acids, -aldehydes, -ketones and gamma-amino alcohols	20031219
EP-1694630-B1	Method for producing chiral or enantiomer-enriched beta-amino acids, -aldehydes, -ketones and gamma-amino alcohols	20031219
US-2007123589-A1	Method for producing chiral or enantiomer-enriched beta-amino acids, aldehydes, ketones and gama-amino alcohols	20031219
WO-2005063682-A1	Improved method for producing chiral or enantiomer-enriched beta-amino acids, -aldehydes, -ketones and gamma-amino alcohols	20031219

Complexity:	102
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	152.094963011
Formal Charge:	0
Heavy Atom Count:	11
Hydrogen Bond Acceptor Count:	3
Hydrogen Bond Donor Count:	2
Isotope Atom Count:	0
Monoisotopic Mass:	152.094963011
Rotatable Bond Count:	3
Topological Polar Surface Area:	59.1
Undefined Atom Stereocenter Count:	1
Undefined Bond Stereocenter Count:	0
XLogP3:	-0.6