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22633-44-9

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22633-44-9 Usage

General Description

3-Bromomethyl-3-oxetanemethanol, also known as 3-Bromo-3-hydroxymethyl-3-methyloxetane, is a chemical compound with the molecular formula C5H9BrO2. It is a colorless liquid with a molecular weight of 177.02 g/mol. 3-Bromomethyl-3-oxetanemethanol is used in the synthesis of various pharmaceuticals and organic compounds. It is also known for its potential use as a versatile intermediate in organic chemistry. 3-Bromomethyl-3-oxetanemethanol is a highly reactive compound and should be handled with care by trained professionals.

Check Digit Verification of cas no

The CAS Registry Mumber 22633-44-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,6,3 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 22633-44:
(7*2)+(6*2)+(5*6)+(4*3)+(3*3)+(2*4)+(1*4)=89
89 % 10 = 9
So 22633-44-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H9BrO2/c6-1-5(2-7)3-8-4-5/h7H,1-4H2

22633-44-9 Well-known Company Product Price

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  • Alfa Aesar

  • (H57413)  3-Bromomethyl-3-oxetanemethanol, 95%   

  • 22633-44-9

  • 250mg

  • 764.0CNY

  • Detail
  • Alfa Aesar

  • (H57413)  3-Bromomethyl-3-oxetanemethanol, 95%   

  • 22633-44-9

  • 500mg

  • 1274.0CNY

  • Detail

22633-44-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Bromomethyl-3-oxetanemethanol

1.2 Other means of identification

Product number -
Other names [3-(Bromomethyl)oxetan-3-yl]methanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:22633-44-9 SDS

22633-44-9Relevant articles and documents

Method for synthesizing p-methoxybenzyl [3-(aminomethyl)-oxetane-3-yl]carbamate p-chlorobenzoate

-

Paragraph 0046; 0047, (2018/05/30)

The invention provides a method for synthesizing p-methoxybenzyl [3-(aminomethyl)-oxetane-3-yl]carbamate p-chlorobenzoate. The method comprises the following steps: a, preparing a compound 2 from a cyclic imido group substituted compound 1, wherein the cyclic imido group is any one of phthalimide, succimide and maleimide; b, carrying out an amination reaction on a primary amine and the compound 2to generate a compound 3; and c, reacting the compound 3 with 4-chlorobenzoic acid to obtain a compound 4. A reaction route is shown in the description. The synthesis method is friendly to the environment, and is suitable for large-scale industrial production.

Synthesis of novel 3-(4-substitutedaryloxymethyl) oxetan-3- ylamines

Shyamsunder Reddy,George Vineel,Naidu,Dubey

, p. 345 - 348 (2019/01/21)

2,2-Bis (bromomethyl) propane-1,3-diol (1) was cyclized in the presence of sodium ethoxide at room temp to obtain (3-(bromomethyl) oxetan-3-yl) methanol (2) which was treated with various phenols (3) to yield (3-(aryloxymethyl) oxetan-3-yl) methanol (4). The latter, on oxidation with KMnO4 in aq. NaOH containing dioxan gave the corresponding carboxylic acid derivatives 5.5 with benzyl alcohol containing Diphenyl Phosphoryl Azide (DPPA) gave 3-(4-substitutedaryloxymethyl) oxetan-3-ylamines (7) via N-CBz protected aminooxetanes (6).

Synthesis of 3,3-disubstituted oxetane building blocks

Vigo, Daniele,Stasi, Luigi,Gagliardi, Stefania

scheme or table, p. 565 - 567 (2011/03/18)

The synthesis of two different sets of 3,3-disubstituted oxetane building blocks is described. These molecules can be usefully incorporated in more complex structures to modulate their metabolic and physicochemical properties. The synthetic pathways are g

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