N-2-Benzyloxyphenyl α-Benzilidene-d5 Isobutyrylacetamide

Base Information

Chemical Name:N-2-Benzyloxyphenyl α-Benzilidene-d5 Isobutyrylacetamide
CAS No.:1020719-18-9
Molecular Formula:C₂₆H₂₅NO₃
Molecular Weight:404.45
Hs Code.:
Mol file:1020719-18-9.mol

Synonyms:

Suppliers and Price of N-2-Benzyloxyphenyl α-Benzilidene-d5 Isobutyrylacetamide

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
Packaging
price

TRC
N-2-Benzyloxyphenylα-Benzilidene-d5Isobutyrylacetamide
50mg
$ 1230.00

Medical Isotopes, Inc.
N-2-Benzyloxyphenylα-Benzilidene-d5Isobutyrylacetamide
1 mg
$ 845.00

American Custom Chemicals Corporation
N-2-BENZYLOXYPHENYL-ALPHA-BENZILIDENE-D5 ISOBUTYRYLACETAMIDE 95.00%
5MG
$ 503.17

Total 2 raw suppliers

Chemical Property of N-2-Benzyloxyphenyl α-Benzilidene-d5 Isobutyrylacetamide

Chemical Property:

Solubility.:Acetone, Chloroform, Dichloromethane, Ethyl Acetate

Purity/Quality:

97% ^*data from raw suppliers

N-2-Benzyloxyphenylα-Benzilidene-d5Isobutyrylacetamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Uses A deuterated intermediate of the metabolite of Atorvastin, a selective, competitive HMG-CoA reductase inhibitor. Atorvastin is the only drug in its class specfically indicated for lowering both elevated LDL-cholesterol and triglycerides in patients with hypercholesterolemia.

Technology Process of N-2-Benzyloxyphenyl α-Benzilidene-d5 Isobutyrylacetamide

There total 3 articles about N-2-Benzyloxyphenyl α-Benzilidene-d5 Isobutyrylacetamide 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:

: 20012-63-9
o-(benzyloxy)aniline

: 1020719-18-9
C₂₆H₂₀⁽²⁾H₅NO₃

Guidance literature:: Multi-step reaction with 2 steps

1: 76 percent / toluene / Heating

2: β-alanine; glacial acetic acid / hexane / Heating

With acetic acid; 3-amino propanoic acid; In hexane; toluene; 1: Acylation / 2: Condensation;
DOI:10.1002/(SICI)1099-1344(20000315)43:3<261::AID-JLCR312>3.0.CO;2-T

Reference yield:

: 4560-41-2
2-benzyloxynitrobenzene

: 1020719-18-9
C₂₆H₂₀⁽²⁾H₅NO₃

Guidance literature:: Multi-step reaction with 3 steps

1: 67 percent / sodium dithionite / methanol

2: 76 percent / toluene / Heating

3: β-alanine; glacial acetic acid / hexane / Heating

With sodium dithionite; acetic acid; 3-amino propanoic acid; In methanol; hexane; toluene; 1: Reduction / 2: Acylation / 3: Condensation;
DOI:10.1002/(SICI)1099-1344(20000315)43:3<261::AID-JLCR312>3.0.CO;2-T