Oxiranecarboxamide, 3-methyl-2-(1-methylethyl)-, (2R,3S)- (9CI)

Base Information

Chemical Name:Oxiranecarboxamide, 3-methyl-2-(1-methylethyl)-, (2R,3S)- (9CI)
CAS No.:200356-09-8
Molecular Formula:C₇H₁₃NO₂
Molecular Weight:143.186
Hs Code.:
Mol file:200356-09-8.mol

Synonyms:Oxiranecarboxamide,3-methyl-2-(1-methylethyl)-, (2R,3S)- (9CI); Oxiranecarboxamide,3-methyl-2-(1-methylethyl)-, (2R-trans)-

Suppliers and Price of Oxiranecarboxamide, 3-methyl-2-(1-methylethyl)-, (2R,3S)- (9CI)

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 1 raw suppliers

Chemical Property of Oxiranecarboxamide, 3-methyl-2-(1-methylethyl)-, (2R,3S)- (9CI)

Chemical Property:

PSA：55.62000
LogP:0.98550

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Oxiranecarboxamide, 3-methyl-2-(1-methylethyl)-, (2R,3S)- (9CI)

There total 3 articles about Oxiranecarboxamide, 3-methyl-2-(1-methylethyl)-, (2R,3S)- (9CI) which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 144694-78-0,144787-35-9
(S₂,R_S)-2-hydroxy-3-[(4-methylphenyl)sulfinyl]-2-isopropylbutanenitrile

: 200356-09-8
(R₂,S₃)-3-methyl-2-i-propyloxirane-2-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) HBF₄, 2.) MeOH / 1.) CH₂Cl₂, RT, 3 h, 2.) CH₂Cl₂, RT, 3 h

2: 70 percent / BF₃*Et₂O, NaI / acetonitrile

3: 1.) Me₃OBF₄, 2.) aq. K₂CO₃ / 1.) CH₂Cl₂, RT, 3 h, 2.) CH₂Cl₂, RT, 17 h

With methanol; tetrafluoroboric acid; boron trifluoride diethyl etherate; trimethoxonium tetrafluoroborate; potassium carbonate; sodium iodide; In acetonitrile;
DOI:10.1016/S0957-4166(97)00457-6

Reference yield:

: 200356-02-1
(2S,3R)-2-Hydroxy-2-isopropyl-3-((S)-toluene-4-sulfinyl)-butyramide

: 200356-09-8
(R₂,S₃)-3-methyl-2-i-propyloxirane-2-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / BF₃*Et₂O, NaI / acetonitrile

2: 1.) Me₃OBF₄, 2.) aq. K₂CO₃ / 1.) CH₂Cl₂, RT, 3 h, 2.) CH₂Cl₂, RT, 17 h

With boron trifluoride diethyl etherate; trimethoxonium tetrafluoroborate; potassium carbonate; sodium iodide; In acetonitrile;
DOI:10.1016/S0957-4166(97)00457-6

Reference yield:

: 144694-85-9
(S₂,R₃)-2-hydroxy-3-[(4-methylphenyl)sulfenyl]-2-isopropylbutanamide

: 200356-09-8
(R₂,S₃)-3-methyl-2-i-propyloxirane-2-carboxamide

Guidance literature:: With trimethoxonium tetrafluoroborate; potassium carbonate; Yield given. Multistep reaction; 1.) CH₂Cl₂, RT, 3 h, 2.) CH₂Cl₂, RT, 17 h;
DOI:10.1016/S0957-4166(97)00457-6