• Product Name3-Hydroxyazetidine hydrochloride
  • CasNo. 18621-18-6
  • MFC3H7NO.HCl
  • MW109.556
  • Purity
  • Appearancewhite crystal
  • Packing
  • Contact usInquiry

Product Details

CasNo: 18621-18-6

MF: C3H7NO.HCl

Appearance: white crystal

Factory Supply Hot Sale 18621-18-6 with Safe Delivery

  • Molecular Formula:C3H7NO.HCl
  • Molecular Weight:109.556
  • Appearance/Colour:white crystal 
  • Vapor Pressure:0.464mmHg at 25°C 
  • Melting Point:90-92 °C 
  • Boiling Point:170.7 °C at 760 mmHg 
  • Flash Point:120.4 °C 
  • PSA:32.26000 
  • LogP:0.08130 

3-Hydroxyazetidine hydrochloride(Cas 18621-18-6) Usage

InChI:InChI=1/C3H7NO.ClH/c5-3-1-4-2-3;/h3-5H,1-2H2;1H

18621-18-6 Relevant articles

Development of an optimized process for the preparation of 1-benzylazetidin-3-ol: An industrially important intermediate for substituted azetidine

Krishna Reddy,Udaykiran,Chintamani,Mahesh Reddy,Kameswararao, Ch.,Madhusudhan

, p. 462 - 466 (2011)

A thoroughly optimized and robust proces...

Novel efficient synthesis of 1-azabicyclo[1.1.0]butane and its application to the synthesis of 1-(1,3-thiazolin-2-yl)azetidine-3-thiol useful for the pendant moiety of an oral 1β-methyicarbapenem antibiotic L- 084

Hayashi, Kazuhiko,Sato, Chisato,Hiki, Shinsuke,Kumagai, Toshio,Tamai, Satoshi,Abe, Takao,Nagao, Yoshimitsu

, p. 3761 - 3764 (1999)

1-Azabicyclo[1.1.0]butane 2 was successf...

Synthetic method of 3-hydroxyazetidine hydrochloride

-

Paragraph 0081-0085; 0088-0090; 0093-0095, (2020/11/05)

The invention discloses a synthetic meth...

3-nitrile methylene azetidine-1-tert-butyl carbonate preparation method

-

Page/Page column 8; 15-18, (2020/02/06)

The invention discloses a 3-nitrile meth...

A N - aryl heterocyclic butane de-aryl method (by machine translation)

-

Paragraph 0022; 0024; 0025; 0027; 0028; 0030; 0031; 0033, (2019/05/28)

The invention discloses an aryl removing...

Method for preparing 3-hydroxyazetidine hydrochloride and tert-butyl 3-hydroxyazetidine-1-carboxylate

-

Paragraph 0057; 0058; 0059; 0060; 0061; 0062; 0063, (2017/08/30)

The invention discloses a method for pre...

18621-18-6 Process route

1-(diphenylmethyl)-3-azetidinol hydrochloride
90604-02-7

1-(diphenylmethyl)-3-azetidinol hydrochloride

azetion-3-ol hydrochloride
18621-18-6

azetion-3-ol hydrochloride

Conditions
Conditions Yield
With hydrogen; palladium on activated charcoal; In ethanol; water; at 20 ℃; for 4h; under 2625.21 Torr;
100%
With palladium hydroxide on carbon; hydrogen; In ethanol; at 20 ℃; for 12h; under 3040.2 Torr; Inert atmosphere;
94%
With hydrogen; palladium hydroxide on carbon; In ethanol; at 20 ℃; for 12h; under 3040.2 Torr;
94%
With hydrogen; palladium(II) hydroxide/carbon; In methanol; for 48h; under 2844.39 Torr;
52%
With hydrogen; palladium hydroxide on carbon; In methanol; for 48h; under 2844.39 Torr;
52%
With hydrogenchloride; hydrogen; palladium on activated charcoal;
 
With hydrogen; palladium dihydroxide; In methanol; for 72h; under 2844.3 Torr;
 
hydrogenchloride
7647-01-0,15364-23-5

hydrogenchloride

1-(diphenylmethyl)-3-hydroxyazetidine
18621-17-5

1-(diphenylmethyl)-3-hydroxyazetidine

azetion-3-ol hydrochloride
18621-18-6

azetion-3-ol hydrochloride

Conditions
Conditions Yield
With hydrogen; 10% palladium on activated carbon; In 1,4-dioxane; methanol; at 60 ℃; for 6h; under 2068.65 Torr;
68%

18621-18-6 Upstream products

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    90604-02-7

    1-(diphenylmethyl)-3-azetidinol hydrochloride

  • 143329-27-5
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    N-acetyl-3-acetoxyazetidine

  • 19540-05-7
    19540-05-7

    1-azabicyclo<1.1.0>butane

  • 7647-01-0
    7647-01-0

    hydrogenchloride

18621-18-6 Downstream products

  • 154010-96-5
    154010-96-5

    1-(p-Toluenesulfonyl)azetidin-3-ol

  • 141890-67-7
    141890-67-7

    3-hydroxy-1-(p-nitrobenzyloxycarbonyl)azetidine

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    161715-27-1

    1-(1,3-thiazolin-2-yl-)azetidin-3-ol

  • 519188-55-7
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    1-(3-(2-(1-benzothiophen-5-yl)ethoxy)propionyl)azetidin-3-ol

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