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(S)-(-)-2-(Boc-Amino)-1,4-butanediol

(S)-(-)-2-(Boc-Amino)-1,4-butanediol Structure
CAS No.
128427-10-1
Chemical Name:
(S)-(-)-2-(Boc-Amino)-1,4-butanediol
Synonyms
(S)-2-Boc-amino-butane-1,4-diol;(S)-2-N-Boc-aMinobutane-1,4-diol;(S)-N-BOC-2-AMINO-BUTANE-1,4-DIOL;(S)-(-)-2-(boc-Amino)-1,4-butendiol;(S)-(-)-N-Boc-2-Amino-1,4-butanediol;(S)-(-)-2-(Boc-Amino)-1,4-butanediol;(S)-N-BOC-2-AMINO-BUTANE-1,4-DIOL ,97%;tert-butyl N-(4,4-dihydroxybutyl)carbaMate;tert-butyl(S)-1,4-dihydroxybutan-2-ylcarbamate;(S)-(-)-2-(Boc-Amino)-1,4-butanediol USP/EP/BP
CBNumber:
CB7504648
Molecular Formula:
C9H19NO4
Molecular Weight:
205.25
MOL File:
128427-10-1.mol
MSDS File:
SDS
Modify Date:
2023/4/23 13:52:06

(S)-(-)-2-(Boc-Amino)-1,4-butanediol Properties

Melting point 65-69 °C(lit.)
Boiling point 365.0±32.0 °C(Predicted)
alpha -8 º (c=1 in chloroform)
Density 1?+-.0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka 11.81±0.46(Predicted)
form Crystalline Powder
color White
optical activity [α]20/D 8°, c = 1 in chloroform

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
Safety Statements  24/25
WGK Germany  3
HS Code  29051990

(S)-(-)-2-(Boc-Amino)-1,4-butanediol price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 536652 (S)-(−)-2-(Boc-amino)-1,4-butanediol 97% 128427-10-1 1G ₹7003.78 2022-06-14 Buy
Sigma-Aldrich(India) 536652 (S)-(−)-2-(Boc-amino)-1,4-butanediol 97% 128427-10-1 5G ₹19896.35 2022-06-14 Buy
Product number Packaging Price Buy
536652 1G ₹7003.78 Buy
536652 5G ₹19896.35 Buy

(S)-(-)-2-(Boc-Amino)-1,4-butanediol Chemical Properties,Uses,Production

Chemical Properties

whitecrystallinepowde

Uses

(S)-(?)-2-(Boc-amino)-1,4-butanediol can be used as a reactant to synthesize:

  • Thiourea-based organocatalysts for asymmetric Michael addition reactions of nitroalkenes to α-nitrocyclohexanone.
  • Bis-copper (II) complex based catalysts for enantioselective Michael reactions.

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tert-butyl N-(1,4-dihydroxybutan-2-yl)carbaMate (S)-2-N-Boc-aMinobutane-1,4-diol tert-butyl N-(4,4-dihydroxybutyl)carbaMate tert-butyl(S)-1,4-dihydroxybutan-2-ylcarbamate Carbamic acid, N-[(1S)-3-hydroxy-1-(hydroxymethyl)propyl]-, 1,1-dimethylethyl ester (S)-(-)-N-Boc-2-Amino-1,4-butanediol Carbamic acid, [(1S)-3-hydroxy-1-(hydroxymethyl)propyl]-, 1,1-dimethylethyl (S)-(-)-2-(boc-Amino)-1,4-butendiol (S)-TERT-BUTYL 1,4-DIHYDROXYBUTAN-2-YLCARBAMATE (S)-N-BOC-2-AMINO-BUTANE-1,4-DIOL ,97% (S)-(-)-2-(Boc-Amino)-1,4-butanediol (S)-(3-Hydroxy-1-hydroxymethylpropyl)carbamic acid tert-butyl ester (S)-2-Boc-amino-butane-1,4-diol tert-butyl N-[(2S)-1,4-dihydroxybutan-2-yl]carbamate (S)-2-(((neopentyloxy)carbonyl)amino)succinic acid (S)-(-)-2-(Boc-Amino)-1,4-butanediol USP/EP/BP (S)-N-BOC-2-AMINO-BUTANE-1,4-DIOL 128427-10-1 HOCH2CH2CHNHCO2CCH33CH2OH N-BOC API intermediates Chiral Compounds Amino Alcohols Chiral Building Blocks Organic Building Blocks