(S)-(+)-2-Amino-1-butanol

(S)-(+)-2-Amino-1-butanol Basic information
Product Name:(S)-(+)-2-Amino-1-butanol
Synonyms:LABOTEST-BB LT01409643;D(+)-2-AMINO-1-BUTANOL;D-2-AMINO-1-BUTANOL;(+/-)-2-AMINO-1-BUTANOL;2-AMINO-1-BUTANOL;(S)-(+)-2-AMINO-1-BUTANOL;(S)(+)-2-AMINOBUTANOL;(S)-2-AMINOBUTANOL
CAS:5856-62-2
MF:C4H11NO
MW:89.14
EINECS:227-475-9
Product Categories:Amino Alcohols;Chiral Building Blocks;Amino Alcohols (Chiral);Chiral Building Blocks;Synthetic Organic Chemistry;Organic Building Blocks;Pharmaceutical Intermediates
Mol File:5856-62-2.mol
(S)-(+)-2-Amino-1-butanol Structure
(S)-(+)-2-Amino-1-butanol Chemical Properties
Melting point -2 °C(lit.)
alpha [α]D20 +9~+11° (neat)
Boiling point 179-183 °C(lit.)
density 0.944 g/mL at 25 °C(lit.)
refractive index n20/D 1.4521(lit.)
Fp 184 °F
storage temp. 2-8°C(protect from light)
solubility Soluble in water
pkapK1: 9.52(+1) (25°C)
form clear liquid
color Clear colorless to slightly yellowish viscous liquid
optical activity[α]20/D +10°, neat
Water Solubility 1000g/L at 25℃
Sensitive Air Sensitive & Hygroscopic
BRN 1718930
CAS DataBase Reference5856-62-2(CAS DataBase Reference)
Safety Information
Hazard Codes C
Risk Statements 34-37-22
Safety Statements 26-36/37/39-45
RIDADR UN 2735 8/PG 3
WGK Germany 3
RTECS EK9625000
HazardClass 8
PackingGroup III
HS Code 29221990
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
(S)-(+)-2-Amino-1-butanol Usage And Synthesis
Chemical Propertiesclear colorless to slightly yellowish viscous
Uses(S)-(+)-2-Amino-1-butanol is a chiral amino alcohol that may be used in the synthesis of (S)-2-(6-benzylamino-9-isopropyl-9H-purin-2-ylamino) butan-1-ol, an (S)-enantiomer of roscovitine. It can also be used to synthesize homochiral 2-methylpyrroles. (S)-(+)-2-Amino-1-butanol is an intermediate for the synthesis of (S,S)-ethambutol, an antibacterial agent for treating tuberculosis.
Purification MethodsThey are purified by shaking with solid NaOH, filtering and distilling through a short column. The oxalate of the racemate has m 176o. They are strong bases and should be stored under N2 in the absence of CO2. The enantiomers have [] 20 ±12.5o (c 2, EtOH). [Johnson & Degering J Org Chem 8 7 1943, Nagao et al. J Org Chem 51 2392 1986, Santaniello et al. J Chem Soc, Perkin Trans 1 919 1985, Beilstein 4 H 291, 4 IV 1705.]
(S)-(+)-2-Amino-1-butanol Preparation Products And Raw materials
Preparation Products(R)-(-)-2-Amino-1-butanol-->(2S)-2-(2-Oxopyrrolidin-1-yl)butanoic acid-->Ethambutol
[R,(+)]-4-(Methylthio)-2-[(9H-purine-6-yl)amino]-1-butanol,[R,(+)]-4-(Methylthio)-2-[(9H-purine-6-yl)amino]-1-butanol 2-Amino-2-methyl-1-propanol 2-[(4-Methylphenylsulfonyl)amino]-1-butanol,2-[(4-Methylphenylsulfonyl)amino]-1-butanol 2-Amino-4-[[(2-chlorobenzo[b]thiophene-1,1-dioxide)-3-yl]amino]-1-butanol,2-Amino-4-[[(2-chlorobenzo[b]thiophene-1,1-dioxide)-3-yl]amino]-1-butanol 4-(Z-AMINO)-1-BUTANOL DL-2-Amino-1-butanol 1-[N-(2-Aminoethyl)-N-[2-[bis(2-aminoethyl)amino]pentyl]amino]-2-butanol,1-[N-(2-Aminoethyl)-N-[2-[bis(2-aminoethyl)amino]pentyl]amino]-2-butanol (-)-4-[Ethyl[(R)-p-methoxy-α-methylphenethyl]amino]-1-butanol,(-)-4-[Ethyl[(R)-p-methoxy-α-methylphenethyl]amino]-1-butanol [R,(-)]-4-Amino-2-butanol,[R,(-)]-4-Amino-2-butanol 2-[[1,3,5-Trimethyl-1H-pyrazolo[4,3-d]pyrimidin-7-yl]amino]-1-butanol,2-[[1,3,5-Trimethyl-1H-pyrazolo[4,3-d]pyrimidin-7-yl]amino]-1-butanol 2-Amino-1-butanol/boric acid,(1:x),2-Amino-1-butanol/boric acid,(1:x) (+)-4-[Ethyl[(S)-p-methoxy-α-methylphenethyl]amino]-1-butanol,(+)-4-[Ethyl[(S)-p-methoxy-α-methylphenethyl]amino]-1-butanol 1-AMINO-2-BUTANOL 1-[N-(2-Aminoethyl)-N-[4-[bis(2-aminoethyl)amino]pentyl]amino]-2-butanol,1-[N-(2-Aminoethyl)-N-[4-[bis(2-aminoethyl)amino]pentyl]amino]-2-butanol 1-[N-(2-Aminoethyl)-N-[4-[bis(2-aminoethyl)amino]butyl]amino]-2-butanol,1-[N-(2-Aminoethyl)-N-[4-[bis(2-aminoethyl)amino]butyl]amino]-2-butanol 1-[N-(2-Aminoethyl)-N-[3-[bis(2-aminoethyl)amino]hexyl]amino]-2-butanol,1-[N-(2-Aminoethyl)-N-[3-[bis(2-aminoethyl)amino]hexyl]amino]-2-butanol 1-[N-(2-Aminoethyl)-N-[4-[bis(2-aminoethyl)amino]hexyl]amino]-2-butanol,1-[N-(2-Aminoethyl)-N-[4-[bis(2-aminoethyl)amino]hexyl]amino]-2-butanol 1-[N-(2-Aminoethyl)-N-[3-[bis(2-aminoethyl)amino]pentyl]amino]-2-butanol,1-[N-(2-Aminoethyl)-N-[3-[bis(2-aminoethyl)amino]pentyl]amino]-2-butanol

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