Skip to Content
Merck
CN
All Photos(1)

Documents

432261

Sigma-Aldrich

(S)-(+)-2-Amino-3-cyclohexyl-1-propanol hydrochloride

97%

Sign Into View Organizational & Contract Pricing

Synonym(s):
(S)-2-Amino-3-cyclohexylpropanol hydrochloride, 3-Cyclohexyl-L-alaninol
Linear Formula:
C6H11CH2CH(NH2)CH2OH·HCl
CAS Number:
Molecular Weight:
193.71
Beilstein:
5288995
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:

Assay

97%

optical activity

[α]20/D +2.6°, c = 1 in methanol

mp

230 °C (dec.) (lit.)

SMILES string

Cl.N[C@H](CO)CC1CCCCC1

InChI

1S/C9H19NO.ClH/c10-9(7-11)6-8-4-2-1-3-5-8;/h8-9,11H,1-7,10H2;1H/t9-;/m0./s1

InChI key

BMHYDTXNZNVADC-FVGYRXGTSA-N

Application

Used in the synthesis of renin inhibitors.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

J R Luly et al.
Journal of medicinal chemistry, 31(12), 2264-2276 (1988-12-01)
The synthesis of diol-containing renin inhibitors has revealed that a simple vicinal diol functionality corresponding to the scissile Leu-Val bond in human angiotensinogen is capable of imparting inhibitory activity at a comparable or higher level than either the corresponding aldehyde

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service