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761460-04-2

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  • SAGECHEM/(S)-tert-Butyl 3-(2-ethoxy-2-oxoethyl)morpholine-4-carboxylate/SAGECHEM/Manufacturer in China

    Cas No: 761460-04-2

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761460-04-2 Usage

General Description

(S)-tert-Butyl 3-(2-ethoxy-2-oxoethyl)morpholine-4-carboxylate is a chemical compound consisting of a morpholine ring with a carboxylate group and a tert-butyl group attached. It also contains a 2-ethoxy-2-oxoethyl side chain. This chemical is often used as an intermediate or building block in the synthesis of pharmaceuticals and agrochemicals. It has potential applications in the development of drugs targeting neurological disorders, cancer, and infectious diseases. Additionally, its unique structure makes it a valuable building block for the production of various organic compounds. Overall, (S)-tert-Butyl 3-(2-ethoxy-2-oxoethyl)morpholine-4-carboxylate is an important chemical compound with diverse potential applications in the field of medicinal and organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 761460-04-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,1,4,6 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 761460-04:
(8*7)+(7*6)+(6*1)+(5*4)+(4*6)+(3*0)+(2*0)+(1*4)=152
152 % 10 = 2
So 761460-04-2 is a valid CAS Registry Number.

761460-04-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl (3S)-3-(2-ethoxy-2-oxoethyl)morpholine-4-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

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

More Details:761460-04-2 SDS

761460-04-2Relevant articles and documents

An efficient synthesis of chiral cyclic β-amino acids via asymmetric hydrogenation

Pousset, Cyrille,Callens, Roland,Marinetti, Angela,Larchevêque, Marc

, p. 2766 - 2770 (2007/10/03)

Cyclic β-amino acids, homoproline, homopipecolic acid and 3-carboxy-methylmorpholine were obtained in high enantiomeric excesses by transition metal-catalyzed asymmetric hydrogenation of cyclic β-acylamino-alkenoates. These compounds were synthesized by a

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