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162698-26-2

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162698-26-2 Usage

General Description

Methyl 2-azetidinecarboxylate hydrochloride is a chemical compound that is commonly used as a building block in organic synthesis. It is a hydrochloride salt of methyl 2-azetidinecarboxylate, which is a derivative of azetidine, a four-membered ring compound containing one nitrogen atom. This chemical is often used in the preparation of pharmaceuticals, agrochemicals, and other fine chemicals due to its reactivity and versatile properties. It can be used as a precursor in the synthesis of various biologically active compounds, making it an important intermediate in the production of valuable chemical products. Additionally, it is important to handle this compound with proper care, as it is classified as a hazardous chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 162698-26-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,6,9 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 162698-26:
(8*1)+(7*6)+(6*2)+(5*6)+(4*9)+(3*8)+(2*2)+(1*6)=162
162 % 10 = 2
So 162698-26-2 is a valid CAS Registry Number.

162698-26-2SDS

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 Methyl azetidine-2-carboxylate hydrochloride

1.2 Other means of identification

Product number -
Other names methyl azetidine-2-carboxylate,hydrochloride

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:162698-26-2 SDS

162698-26-2Downstream Products

162698-26-2Relevant articles and documents

Carbonyl azetidine substituted naphthalimide fluorescent dye as well as synthesis method and application thereof

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Paragraph 0073-0077, (2021/06/13)

The invention provides a novel carbonyl azetidine substituted naphthalimide fluorescent dye as well as synthesis and application thereof. The dye takes 1, 8-naphthalimide as a fluorophore parent, and the fourth site of the 1, 8-naphthalimide is covalently connected with carbonyl azetidine. The novel fluorescent dye has excellent fluorescence intensity and light stability, so that the novel fluorescent dye has wide application prospects in the fields of fluorescence detection, fluorescence imaging and the like, especially in the emerging fields of single molecule detection, super-resolution fluorescence imaging and the like. R1 is H, C1-4 alkyl and aryl, R2 is shown in the specification, and in R2, X1 is H, C1-2 alkyl, X2 is C1-2 alkyl or shown in the specification, X3 is C1-2 alkyl or shown in the specification, and X4 is C1-2 alkyl.

Carbonyl azetidine substituted NBD fluorescent dye as well as synthesis method and application thereof

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Paragraph 0047-0051, (2021/06/12)

The invention provides a novel carbonyl azetidine substituted NBD fluorescent dye as well as synthesis and application thereof. The structure of the dye is characterized in that carbonyl azetidine is covalently connected to the fourth site of a 4-chloro-7-nitrobenzene-2-oxa-1, 3-diazole (NBD) parent. The novel fluorescent dye has excellent fluorescence intensity and light stability, so that the novel fluorescent dye has wide application prospects in the fields of fluorescence detection, fluorescence imaging and the like, especially in the emerging fields of single molecule detection, super-resolution fluorescence imaging and the like. R1 is as described in the specification, X1 is H or C1-2 alkyl, X2 is C1-2 alkyl or as described in the specification, x3 is C1-2 alkyl or as described in the specification, and X4 is C1-2 alkyl.

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