C₄H₄O₄*C₃₂H₃₄⁽²⁾H₅NO₂

Base Information

Chemical Name:C₄H₄O₄*C₃₂H₃₄⁽²⁾H₅NO₂
CAS No.:1316815-02-7
Molecular Formula:C₄H₄O₄*C₃₂H₃₉NO₂
Molecular Weight:590.701
Hs Code.:

C<sub>4</sub>H<sub>4</sub>O<sub>4</sub>*C<sub>32</sub>H<sub>34</sub><sup>(2)</sup>H<sub>5</sub>NO<sub>2</sub>

Synonyms:C₄H₄O₄*C₃₂H₃₄⁽²⁾H₅NO₂

Suppliers and Price of C₄H₄O₄*C₃₂H₃₄⁽²⁾H₅NO₂

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

American Custom Chemicals Corporation
EBASTINE-D5-FUMARATE 95.00%
5MG
$ 499.80

Total 3 raw suppliers

Chemical Property of C₄H₄O₄*C₃₂H₃₄⁽²⁾H₅NO₂

Chemical Property:

Purity/Quality:

95% ^*data from raw suppliers

EBASTINE-D5-FUMARATE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₄H₄O₄*C₃₂H₃₄⁽²⁾H₅NO₂

There total 8 articles about C₄H₄O₄*C₃₂H₃₄⁽²⁾H₅NO₂ 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: 92.0%

: 1216953-13-7
C₃₂H₃₄⁽²⁾H₅NO₂

: 110-17-8,26099-09-2
(2E)-but-2-enedioic acid

: 1316815-02-7
C₄H₄O₄*C₃₂H₃₄⁽²⁾H₅NO₂

Guidance literature:: In ethanol; at 20 ℃;
DOI:10.1002/jlcr.1877

Reference yield:

: 103730-93-4
1-benzylbenzene-2,3,4,5,6-d₅

: 1316815-02-7
C₄H₄O₄*C₃₂H₃₄⁽²⁾H₅NO₂

Guidance literature:: Multi-step reaction with 3 steps

1: N-Bromosuccinimide; dibenzoyl peroxide / tetrachloromethane / 80 °C

2: sodium carbonate / toluene / 6 h / 125 °C

3: ethanol / 20 °C

With N-Bromosuccinimide; sodium carbonate; dibenzoyl peroxide; In tetrachloromethane; ethanol; toluene;
DOI:10.1002/jlcr.1877

Reference yield:

: 2694-78-2
2,3,4,5,6-Pentadeuteriobenzophenon

: 1316815-02-7
C₄H₄O₄*C₃₂H₃₄⁽²⁾H₅NO₂

Guidance literature:: Multi-step reaction with 4 steps

1: palladium 10% on activated carbon; hydrogen / methanol / 12 h / 20 °C

2: N-Bromosuccinimide; dibenzoyl peroxide / tetrachloromethane / 80 °C

3: sodium carbonate / toluene / 6 h / 125 °C

4: ethanol / 20 °C

With N-Bromosuccinimide; palladium 10% on activated carbon; hydrogen; sodium carbonate; dibenzoyl peroxide; In methanol; tetrachloromethane; ethanol; toluene;
DOI:10.1002/jlcr.1877