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106973-40-4

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106973-40-4 Usage

General Description

(S)-Ethyl 4-benzyl-5-oxo-morpholine-3-carboxylate is a chemical compound with the molecular formula C16H19NO4. It is a morpholine derivative containing an ethyl ester group, a benzyl group, and a carboxylate group. (S)-ETHYL 4-BENZYL-5-OXO-MORPHOLINE-3-CARBOXYLATE has potential applications in medicinal chemistry and drug development due to its morpholine ring, which is present in many biologically active compounds. Additionally, the benzyl group and the carboxylate ester moiety can contribute to the compound's pharmacological properties and potential use in drug design. Further research may be warranted to determine the specific activities and potential therapeutic applications of (S)-ethyl 4-benzyl-5-oxo-morpholine-3-carboxylate.

Check Digit Verification of cas no

The CAS Registry Mumber 106973-40-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,9,7 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 106973-40:
(8*1)+(7*0)+(6*6)+(5*9)+(4*7)+(3*3)+(2*4)+(1*0)=134
134 % 10 = 4
So 106973-40-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H17NO4/c1-2-19-14(17)12-9-18-10-13(16)15(12)8-11-6-4-3-5-7-11/h3-7,12H,2,8-10H2,1H3/t12-/m0/s1

106973-40-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl (3S)-4-benzyl-5-oxomorpholine-3-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl (S)-5-oxo-4-(phenylmethyl)morpholine-3-carboxylate

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:106973-40-4 SDS

106973-40-4Relevant articles and documents

Properties and Reactions of Substituted 1,2-Thiazetidine 1,1-Dioxides: Chiral Mono- and Bicyclic 1,2-Thiazetidine 1,1-Dioxides from α-Amino Acids

Meinzer, Alexandra,Breckel, Andrea,Thaher, Bassam Abu,Manicone, Nico,Otto, Hans-Hartwig

, p. 90 - 105 (2007/10/03)

New chiral mono- and bicyclic β-sultams, valuable building blocks for drug synthesis, have been prepared from L-Ala, L-Val, L-Leu, L-Ile, L-Phe, L-Cys, L-Ser, L-Thr, and D-penicillamine by transformation of the COOH group into a methylsulfonyl chloride function, followed by cyclization under basic conditions. Selected properties, derivatives, and reactions of the β-sultams are described.

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