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1-BOC-3-[(4-BROMOPHENYL-AMINO)-METHYL]-AZETIDINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

887589-74-4

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887589-74-4 Usage

Azetidine derivative

Four-membered heterocyclic compound with one nitrogen atom
Azetidine is the core structure of 1-BOC-3-[(4-BROMOPHENYL-AMINO)-METHYL]-AZETIDINE, providing a unique ring system that can influence its reactivity and properties.

BOC protective group

tert-butyloxycarbonyl group attached to the amine group
The BOC group is commonly used to protect amine groups during chemical reactions, preventing unwanted side reactions and allowing for selective deprotection later.

4-Bromophenyl group

Attached to the carbon of the azetidine ring
The presence of the 4-bromophenyl group introduces a bromine atom, which can affect the compound's reactivity, stability, and potential applications.

Potential applications

Organic synthesis and drug development
The unique properties and reactivity of the azetidine ring make 1-BOC-3-[(4-BROMOPHENYL-AMINO)-METHYL]-AZETIDINE a candidate for use in the synthesis of complex organic molecules and as a building block in the development of new pharmaceuticals.

Reactivity

Influenced by the azetidine ring and the presence of the BOC and 4-bromophenyl groups
The reactivity of 1-BOC-3-[(4-BROMOPHENYL-AMINO)-METHYL]-AZETIDINE is determined by the electronic and steric effects of the various functional groups, which can be exploited in chemical reactions and drug design.

Structural features

Amino group, bromine atom, and carbonyl group

Stereochemistry

Potential for stereoisomers due to the presence of a chiral center
The compound may exist as different stereoisomers, which can have distinct properties and reactivities, depending on the spatial arrangement of the atoms around the chiral center.

Solubility

Likely soluble in organic solvents, such as dichloromethane, ethyl acetate, or methanol
The solubility of the compound can be influenced by the presence of the BOC group and the 4-bromophenyl group, which can affect its interactions with various solvents.

Stability

May be sensitive to acidic or basic conditions due to the presence of the BOC group
The BOC protective group can be removed under acidic conditions, which may affect the stability of the compound in the presence of strong acids or bases.

Check Digit Verification of cas no

The CAS Registry Mumber 887589-74-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,7,5,8 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 887589-74:
(8*8)+(7*8)+(6*7)+(5*5)+(4*8)+(3*9)+(2*7)+(1*4)=264
264 % 10 = 4
So 887589-74-4 is a valid CAS Registry Number.

887589-74-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 3-[(4-bromoanilino)methyl]azetidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names -

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:887589-74-4 SDS

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