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Carbamic acid, [[5-[acetyl(phenylmethyl)amino]-4-(phenylmethyl)-2-oxazolyl]methyl]-, phenylmethyl ester

Base Information Edit
  • Chemical Name:Carbamic acid, [[5-[acetyl(phenylmethyl)amino]-4-(phenylmethyl)-2-oxazolyl]methyl]-, phenylmethyl ester
  • CAS No.:87783-95-7
  • Molecular Formula:C28H27N3O4
  • Molecular Weight:469.54
  • Hs Code.:
  • Mol file:87783-95-7.mol
Carbamic acid,
[[5-[acetyl(phenylmethyl)amino]-4-(phenylmethyl)-2-oxazolyl]methyl]-,
phenylmethyl ester

Synonyms:

Suppliers and Price of Carbamic acid, [[5-[acetyl(phenylmethyl)amino]-4-(phenylmethyl)-2-oxazolyl]methyl]-, phenylmethyl ester
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Carbamic acid, [[5-[acetyl(phenylmethyl)amino]-4-(phenylmethyl)-2-oxazolyl]methyl]-, phenylmethyl ester Edit
Chemical Property:
Purity/Quality:
Safty Information:
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MSDS Files:

SDS file from LookChem

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Technology Process of Carbamic acid, [[5-[acetyl(phenylmethyl)amino]-4-(phenylmethyl)-2-oxazolyl]methyl]-, phenylmethyl ester

There total 6 articles about Carbamic acid, [[5-[acetyl(phenylmethyl)amino]-4-(phenylmethyl)-2-oxazolyl]methyl]-, phenylmethyl ester 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:
Guidance literature:
With tetrabutyl-ammonium chloride; sodium hydride; 1.) THF, 0 deg C, 15 min, 2.) RT, 1 h;
DOI:10.1021/ja00364a041
Guidance literature:
Multi-step reaction with 3 steps
1: 880 mg / tetrahydrofuran / 6 h / Ambient temperature
2: 69 percent / BF3*Et2O / CHCl3 / 6 h / 0 °C
3: 76 percent / 1.) NaH, Bu4NCl / 1.) THF, 0 deg C, 15 min, 2.) RT, 1 h
With boron trifluoride diethyl etherate; tetrabutyl-ammonium chloride; sodium hydride; In tetrahydrofuran; chloroform;
DOI:10.1021/ja00364a041
Guidance literature:
Multi-step reaction with 4 steps
1: 1.) NH4Cl, NH4OH, 2.) HCl gas / 1.) H2O-Et2O, RT, 2.) Et2O, 0 deg C
2: 880 mg / tetrahydrofuran / 6 h / Ambient temperature
3: 69 percent / BF3*Et2O / CHCl3 / 6 h / 0 °C
4: 76 percent / 1.) NaH, Bu4NCl / 1.) THF, 0 deg C, 15 min, 2.) RT, 1 h
With hydrogenchloride; ammonium hydroxide; boron trifluoride diethyl etherate; tetrabutyl-ammonium chloride; sodium hydride; ammonium chloride; In tetrahydrofuran; chloroform;
DOI:10.1021/ja00364a041
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