4-Nitrobenzyl dodecanoate

Base Information

Chemical Name:4-Nitrobenzyl dodecanoate
CAS No.:4457-34-5
Molecular Formula:C₁₉H₂₉NO₄
Molecular Weight:335.444
Hs Code.:
DSSTox Substance ID:DTXSID901034297

Synonyms:4457-34-5;4-Nitrobenzyl dodecanoate;DTXSID901034297;Dodecanoic acid, (4-nitrophenyl)methyl ester

Suppliers and Price of 4-Nitrobenzyl dodecanoate

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

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Chemical Property of 4-Nitrobenzyl dodecanoate

Chemical Property:

XLogP3:6.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:13
Exact Mass:335.20965841
Heavy Atom Count:24
Complexity:346

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCCCCCCCCC(=O)OCC1=CC=C(C=C1)[N+](=O)[O-]

Technology Process of 4-Nitrobenzyl dodecanoate

There total 4 articles about 4-Nitrobenzyl dodecanoate 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:

: 1255952-65-8
(S)-jalapinolic acid 11-O-(2-O-trans-cinnamoyl)-[(4-O-n-dodecanoyl)]-α-L-rhamnopyranosyl-(1->4)-O-(2-O-n-dodecanoyl)-α-L-rhamnopyranosyl-(1->4)-O-α-L-rhamnopyranosyl-(1->2)-O-β-D-fucopyranoside intramolecular 1,2''-ester

: 2978-11-2
p-nitrobenzyl-N,N′-diisopropylisourea

: 4457-34-5
Laurinsaeure-p-nitro-benzylester

: 116990-79-5
p-nitrobenzyl (E)-cinnamate

Guidance literature:: (S)-jalapinolic acid 11-O-(2-O-trans-cinnamoyl)-[(4-O-n-dodecanoyl)]-α-L-rhamnopyranosyl-(1->4)-O-(2-O-n-dodecanoyl)-α-L-rhamnopyranosyl-(1->4)-O-α-L-rhamnopyranosyl-(1->2)-O-β-D-fucopyranoside intramolecular 1,2''-ester; With water; potassium hydroxide; In methanol; at 90 ℃; for 2h;

p-nitrobenzyl-N,N′-diisopropylisourea; In dichloromethane; at 80 ℃; for 2h;
DOI:10.1021/np100283t

Reference yield:

: 1255952-64-7
(S)-jalapinolic acid 11-O-(2-O-trans-cinnamoyl)-[(4-O-n-dodecanoyl)]-α-L-rhamnopyranosyl-(1->4)-O-(3-O-n-decanoyl)-α-L-rhamnopyranosyl-(1->4)-O-α-L-rhamnopyranosyl-(1->2)-O-β-D-fucopyranoside intramolecular 1,2''-ester

: 2978-11-2
p-nitrobenzyl-N,N′-diisopropylisourea

: 35300-60-8
Caprinsaeure-p-nitrobenzylester

: 4457-34-5
Laurinsaeure-p-nitro-benzylester

: 116990-79-5
p-nitrobenzyl (E)-cinnamate

Guidance literature:: (S)-jalapinolic acid 11-O-(2-O-trans-cinnamoyl)-[(4-O-n-dodecanoyl)]-α-L-rhamnopyranosyl-(1->4)-O-(3-O-n-decanoyl)-α-L-rhamnopyranosyl-(1->4)-O-α-L-rhamnopyranosyl-(1->2)-O-β-D-fucopyranoside intramolecular 1,2''-ester; With water; potassium hydroxide; In methanol; at 90 ℃; for 2h;

p-nitrobenzyl-N,N′-diisopropylisourea; In dichloromethane; at 80 ℃; for 2h;
DOI:10.1021/np100283t

Reference yield:

: 1255952-66-9
(S)-jalapinolic acid 11-O-(2-O-trans-cinnamoyl)-[(4-O-n-dodecanoyl)]-α-L-rhamnopyranosyl-(1->4)-O-(2-O-n-decanoyl)-α-L-rhamnopyranosyl-(1->4)-O-α-L-rhamnopyranosyl-(1->2)-O-β-D-fucopyranoside intramolecular 1,3''-ester

: 2978-11-2
p-nitrobenzyl-N,N′-diisopropylisourea

: 35300-60-8
Caprinsaeure-p-nitrobenzylester

: 4457-34-5
Laurinsaeure-p-nitro-benzylester

: 116990-79-5
p-nitrobenzyl (E)-cinnamate

Guidance literature:: (S)-jalapinolic acid 11-O-(2-O-trans-cinnamoyl)-[(4-O-n-dodecanoyl)]-α-L-rhamnopyranosyl-(1->4)-O-(2-O-n-decanoyl)-α-L-rhamnopyranosyl-(1->4)-O-α-L-rhamnopyranosyl-(1->2)-O-β-D-fucopyranoside intramolecular 1,3''-ester; With water; potassium hydroxide; In methanol; at 90 ℃; for 2h;

p-nitrobenzyl-N,N′-diisopropylisourea; In dichloromethane; at 80 ℃; for 2h;
DOI:10.1021/np100283t