(S)-(+)-Isoleucinol, 97%

Name: (S)-(+)-Isoleucinol, 97% | 24629-25-2
Brand: J&K Chemical
SKU: JK339649_25_G
Price: 31.73 USD
Availability: OutOfStock

Cat. No JK339649_25_G

Vendor: J&K Chemical

Product Information

Product Name

(S)-(+)-Isoleucinol, 97%

Brand Name

J&K

Product Number

339649

CAS

24629-25-2

Molecular Formula

C6H15NO

Molecular Weight

117.19

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

(2S,3S)-2-Amino-3-methyl-1-pentanol L-Isoleucinol

PubChem CID

91202

IUPAC Name

2-amino-3-methylpentan-1-ol

InChI Key

VTQHAQXFSHDMHT-UHFFFAOYSA-N

SMILES

CCC(C)C(CO)N

Properties

Melting Point

36-39

Boiling Point

Flash Point

100

n20D

1.4589

Optical Activity

+3.5 to +5.5 (C=1.6, MeOH)

Safety Information

Precautionary Statement

P262

References Data Source From Pubchem

Synthesis of N-heterocycles through alcohol dehydrogenative coupling

Publication Name: Nature Protocols

Publication Date: 2024-08-22

DOI: 10.1038/s41596-024-01031-w

Synthesis and luminescence properties of novel carbazolyl-containing amino alcohol Schiff bases

Publication Name: Research on Chemical Intermediates

Publication Date: 2013-08-27

DOI: 10.1007/s11164-013-1371-1

A Catalyst-Free, Convenient Construction of Eight-Membered [1,4]Oxazocane-5,8-dione Heterocycles from Aminoethanols with Divinyl Succinate

Publication Name: Synlett

Publication Date: 2008-07-02

DOI: 10.1055/s-2008-1078572

An atom counting and electrophilicity based QSTR approach

Publication Name: Journal of Chemical Sciences

Publication Date: 2007-09

DOI: 10.1007/s12039-007-0061-1

(S)-(+)-Isoleucinol, 97%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Synthesis of N-heterocycles through alcohol dehydrogenative coupling

Synthesis and luminescence properties of novel carbazolyl-containing amino alcohol Schiff bases

A Catalyst-Free, Convenient Construction of Eight-Membered [1,4]Oxazocane-5,8-dione Heterocycles from Aminoethanols with Divinyl Succinate

An atom counting and electrophilicity based QSTR approach

(S)-(+)-Isoleucinol, 97%

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3-methoxy-L-phenylalanine

2-Ethynyl-1,3,5-trimethylbenzene, 97%

Tris-acetic acid electrophoresis buffer (50×TAE)

[S(R)]-N-[(1S)-1-[2-(Diadamantanphosphino)phenyl]ethyl]-N,2-dimethyl-2-propanesulfinamide, 95%

Mycophenolate Mofetil EP Impurity H

3-(4-Bromo-2-fluoro-3-methoxyphenyl)-3-oxo-propionic acid ethyl ester

Isochroman-1-carboxylic acid

Mycophenolate Mofetil

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(S)-(+)-Isoleucinol, 97%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Synthesis of N-heterocycles through alcohol dehydrogenative coupling

Synthesis and luminescence properties of novel carbazolyl-containing amino alcohol Schiff bases

A Catalyst-Free, Convenient Construction of Eight-Membered [1,4]Oxazocane-5,8-dione Heterocycles from Aminoethanols with Divinyl Succinate

An atom counting and electrophilicity based QSTR approach

(S)-(+)-Isoleucinol, 97%

Related Product

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3-methoxy-L-phenylalanine

2-Ethynyl-1,3,5-trimethylbenzene, 97%

Tris-acetic acid electrophoresis buffer (50×TAE)

[S(R)]-N-[(1S)-1-[2-(Diadamantanphosphino)phenyl]ethyl]-N,2-dimethyl-2-propanesulfinamide, 95%

Mycophenolate Mofetil EP Impurity H

3-(4-Bromo-2-fluoro-3-methoxyphenyl)-3-oxo-propionic acid ethyl ester

Isochroman-1-carboxylic acid

Mycophenolate Mofetil

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