1H-1,4-Diazepine, hexahydro-1,4-bis((4E)-5-(3,4,5-trimethoxyphenyl)-4-penten-1-yl)-

Base Information

Chemical Name:1H-1,4-Diazepine, hexahydro-1,4-bis((4E)-5-(3,4,5-trimethoxyphenyl)-4-penten-1-yl)-
CAS No.:191089-59-5
Deprecated CAS:286441-08-5
Molecular Formula:C33H48N2O6
Molecular Weight:568.76031
Hs Code.:
UNII:36376CA57N
Nikkaji Number:J1.333.967H
Wikidata:Q27256515
Mol file:191089-59-5.mol

Synonyms:K 7174;K-7174

Suppliers and Price of 1H-1,4-Diazepine, hexahydro-1,4-bis((4E)-5-(3,4,5-trimethoxyphenyl)-4-penten-1-yl)-

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

DC Chemicals
K-7174 >98%
50 mg
$ 280.00

DC Chemicals
K-7174 >98%
10 mg
$ 120.00

Crysdot
K-7174 98+%
10mg
$ 115.00

Crysdot
K-7174 98+%
5mg
$ 76.00

Crysdot
K-7174 98+%
50mg
$ 451.00

Biorbyt Ltd
K-7174
50 mg
$ 569.50

Biorbyt Ltd
K-7174
10 mg
$ 324.70

Total 8 raw suppliers

Chemical Property of 1H-1,4-Diazepine, hexahydro-1,4-bis((4E)-5-(3,4,5-trimethoxyphenyl)-4-penten-1-yl)-

Chemical Property:

PSA：61.86000
LogP:5.90870
Storage Temp.:2-8°C
XLogP3:6.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:16
Exact Mass:568.35123726
Heavy Atom Count:41
Complexity:663

Purity/Quality:

98% ^*data from raw suppliers

K-7174 >98% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC(=CC(=C1OC)OC)C=CCCCN2CCCN(CC2)CCCC=CC3=CC(=C(C(=C3)OC)OC)OC
Isomeric SMILES:COC1=CC(=CC(=C1OC)OC)/C=C/CCCN2CCN(CCC2)CCC/C=C/C3=CC(=C(C(=C3)OC)OC)OC

Technology Process of 1H-1,4-Diazepine, hexahydro-1,4-bis((4E)-5-(3,4,5-trimethoxyphenyl)-4-penten-1-yl)-

There total 3 articles about 1H-1,4-Diazepine, hexahydro-1,4-bis((4E)-5-(3,4,5-trimethoxyphenyl)-4-penten-1-yl)- 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: 59.0%

: 505-66-8
1,4-Diazacycloheptane

: 191089-65-3
(E)-5-(3,4,5-trimethoxyphenyl)-4-pentenyl bromide

: 191089-59-5
1,4-bis((E)-5-(3,4,5-trimethoxyphenyl)pent-4-enyl)-1,4-diazepane

Guidance literature:: With potassium carbonate; potassium iodide; In acetonitrile; for 7h; Reflux;
DOI:10.5012/bkcs.2012.33.9.2903

Reference yield:

: 505-66-8
1,4-Diazacycloheptane

: 191089-65-3
(E)-5-(3,4,5-trimethoxyphenyl)-4-pentenyl bromide

: 144-55-8
sodium hydrogencarbonate

: 191089-59-5
1,4-bis((E)-5-(3,4,5-trimethoxyphenyl)pent-4-enyl)-1,4-diazepane

Guidance literature:: With hydrogenchloride; potassium iodide; potassium carbonate; In 1,4-dioxane; N-methyl-acetamide; ethyl acetate;

Reference yield:

: C₁₄H₁₉BrO₃

: 191089-59-5
1,4-bis((E)-5-(3,4,5-trimethoxyphenyl)pent-4-enyl)-1,4-diazepane

Guidance literature:: Multi-step reaction with 2 steps

1: iodine / acetonitrile / 2 h / Reflux

2: potassium carbonate; potassium iodide / acetonitrile / 7 h / Reflux

With iodine; potassium carbonate; potassium iodide; In acetonitrile;
DOI:10.5012/bkcs.2012.33.9.2903