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(S)-(-)-2-METHOXYPROPIONAMIDE, 98, also known as (S)-(-)-2-Methoxypropionamide (CAS# 336111-20-7), is a yellow solid compound that is useful in organic synthesis. It plays a significant role in the creation of various chemical compounds and has potential applications across different industries.

336111-20-7

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336111-20-7 Usage

Uses

Used in Organic Synthesis:
(S)-(-)-2-METHOXYPROPIONAMIDE, 98 is used as a synthetic building block for the development of new chemical compounds. Its unique structure allows it to be a valuable component in the synthesis of various organic molecules, contributing to the advancement of chemical research and product development.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (S)-(-)-2-METHOXYPROPIONAMIDE, 98 is used as an intermediate in the synthesis of pharmaceutical compounds. Its properties make it a suitable candidate for the development of new drugs and medications, potentially leading to innovative treatments for various medical conditions.
Used in Chemical Research:
(S)-(-)-2-METHOXYPROPIONAMIDE, 98 is also utilized in chemical research as a tool to study the properties and behavior of different compounds. Its unique structure and reactivity can provide valuable insights into the mechanisms of various chemical reactions, furthering our understanding of organic chemistry.
Used in Material Science:
In the field of material science, (S)-(-)-2-METHOXYPROPIONAMIDE, 98 can be used as a component in the development of new materials with specific properties. Its incorporation into the synthesis process can lead to the creation of materials with enhanced characteristics, such as improved stability, reactivity, or functionality.
Overall, (S)-(-)-2-METHOXYPROPIONAMIDE, 98 is a versatile compound with a wide range of applications across various industries, including organic synthesis, pharmaceuticals, chemical research, and material science. Its unique properties and potential uses make it an important compound for further exploration and development.

Check Digit Verification of cas no

The CAS Registry Mumber 336111-20-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,6,1,1 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 336111-20:
(8*3)+(7*3)+(6*6)+(5*1)+(4*1)+(3*1)+(2*2)+(1*0)=97
97 % 10 = 7
So 336111-20-7 is a valid CAS Registry Number.
InChI:InChI=1/C4H9NO2/c1-3(7-2)4(5)6/h3H,1-2H3,(H2,5,6)/t3-/m0/s1

336111-20-7SDS

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 (2S)-2-methoxypropanamide

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:336111-20-7 SDS

336111-20-7Downstream Products

336111-20-7Relevant academic research and scientific papers

The Influence of Borate Buffers on the Hydration Rate of Cyanohydrins: Evidence for an Intramolecular Mechanism

Jammot, Jacqueline,Pascal, Robert,Commeyras, Auguste

, p. 157 - 162 (2007/10/02)

The effects of borate buffers on the pseudo first-order rate constants for the hydration of hydroxyacetonitrile (1) have been examined on the pH range 8.6-10.3 at 80 deg C.Kinetic results are compatible with a reaction of the neutral cyanohydrin with borate anion or any other kinetically equivalent mechanism.Cyanohydrin structural effects are consistent with a pathway involving the pre-equilibrium formation of a borate-substrate adduct, followed by a rate-determining intramolecular nucleophilic attack on the nitrile group.Phenylboronate ion has also been shown to act as an efficient catalyst, but it was not possible to detect any influence due to disubstituted borate ions.Thus, it is suggested that a trigonal borate anion actually acts as a nucleophile.

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