TERT-BUTOXYCARBONYLAMINO-(4-NITRO-PHENYL)-ACETIC ACID

Base Information

Chemical Name:TERT-BUTOXYCARBONYLAMINO-(4-NITRO-PHENYL)-ACETIC ACID
CAS No.:115116-80-8
Molecular Formula:C₁₃H₁₆N₂O₆
Molecular Weight:296.28
Hs Code.:2924299090
Mol file:115116-80-8.mol

Synonyms:Benzeneaceticacid, a-[[(1,1-dimethylethoxy)carbonyl]amino]-4-nitro-,(?à)-

Suppliers and Price of TERT-BUTOXYCARBONYLAMINO-(4-NITRO-PHENYL)-ACETIC ACID

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
TERT-BUTOXYCARBONYLAMINO-(4-NITRO-PHENYL)-ACETIC ACID 95.00%
5MG
$ 505.77

Total 8 raw suppliers

Chemical Property of TERT-BUTOXYCARBONYLAMINO-(4-NITRO-PHENYL)-ACETIC ACID

Chemical Property:

PSA：121.45000
LogP:3.15930

Purity/Quality:

98%min ^*data from raw suppliers

TERT-BUTOXYCARBONYLAMINO-(4-NITRO-PHENYL)-ACETIC ACID 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of TERT-BUTOXYCARBONYLAMINO-(4-NITRO-PHENYL)-ACETIC ACID

There total 1 articles about TERT-BUTOXYCARBONYLAMINO-(4-NITRO-PHENYL)-ACETIC ACID 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: 70.0%

: 58632-95-4
2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrile

: 5407-25-0
2-amino-2-(4-nitrophenyl)acetic acid

: 115116-80-8
tert-butoxycarbonyl-p-nitro-DL-phenylglycine

Guidance literature:: DOI:10.1248/cpb.36.1205

Reference yield:

: 115116-80-8
tert-butoxycarbonyl-p-nitro-DL-phenylglycine

: 115087-95-1
β-naphthylamide of p-guanidino-DL-phenylglycine hydrochloride

Guidance literature:: Multi-step reaction with 6 steps

1: catalytic reduction

2: guanidination

3: 86 percent / HCl, formic acid, anisole / dioxane / 20 h / 0 °C

4: 70 percent

5: 35 percent

6: 92 percent / hydrogen / palladium black / methanol / 24 h / Ambient temperature

With hydrogenchloride; formic acid; hydrogen; methoxybenzene; palladium; In 1,4-dioxane; methanol;
DOI:10.1248/cpb.36.1205

Reference yield:

: 115116-80-8
tert-butoxycarbonyl-p-nitro-DL-phenylglycine

: 115087-94-0
Benzyloxycarbonylamino-(4-guanidino-phenyl)-acetic acid

Guidance literature:: Multi-step reaction with 4 steps

1: catalytic reduction

2: guanidination

3: 86 percent / HCl, formic acid, anisole / dioxane / 20 h / 0 °C

4: 70 percent

With hydrogenchloride; formic acid; methoxybenzene; In 1,4-dioxane;
DOI:10.1248/cpb.36.1205