Home > Compound List > Product Information
L-Valinol_Molecular_structure_CAS_2026-48-4)
Click picture or here to close

L-Valinol

Catalog No. 94672 Name Sigma Aldrich
CAS Number 2026-48-4 Website http://www.sigmaaldrich.com
M. F. C5H13NO Telephone 1-800-521-8956
M. W. 103.16282 Fax
Purity ≥97.0% (GC/NT) Email
Storage Chembase ID: 3975

SYNONYMS

Title
L-缬氨醇
IUPAC name
(2S)-2-amino-3-methylbutan-1-ol
IUPAC Traditional name
L-valinol
Synonyms
(S)-(+)-2-氨基-3-甲基-1-丁醇
(S)-(+)-2-Amino-3-methyl-1-butanol

DATABASE IDS

EC Number 217-975-5
Beilstein Number 1719137
MDL Number MFCD00064296
CAS Number 2026-48-4
PubChem SID 24890042

PROPERTIES

Empirical Formula (Hill Notation) C5H13NO
Grade purum
Purity ≥97.0% (GC/NT)
Boiling Point 189-190 °C(lit.)
Flash Point 78 °C
Flash Point 172.4 °F
Melting Point 30-34 °C
Optical Rotation [α]20/D +10±1°, c = 10% in H2O
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H319
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P305 + P351 + P338
Risk Statements 36
Safety Statements 26
Storage Temperature 2-8°C
German water hazard class 3

DETAILS

Description (English)
Other Notes
Important chiral auxiliary and building block; preparation of 4-isopropyloxazolidinones, employed in stereocontrolled aldol and alkylation reactions 1; Synthesis of chiral 2-thiazolidinethiones for aldol reactions 2; Asymmetric alkylation of condensation product with keto acids 3; Asymmetric reactions of its amidines and imines 4; Oxidation of N-protected derivative to the aldehyde 5
Description (简体中文)
Other Notes
重要的手性助剂和结构单元;制备用于立体控制性羟醛反应和烷基化反应的 4-异丙基噁唑烷酮1;合成用于羟醛反应的手性 2-噻唑烷硫酮2;酮酸与其缩合产物进行不对称烷基化反应3;它对应的脒和亚胺的不对称性反应4;将 N-保护衍生物氧化为醛5

REFERENCES