N-(4-(3-oxo-6-amino-2,3-dihydro-1,2,4-benzotriazin-2-yl)benzoyl)glutamic acid

Base Information

Chemical Name:N-(4-(3-oxo-6-amino-2,3-dihydro-1,2,4-benzotriazin-2-yl)benzoyl)glutamic acid
CAS No.:122712-57-6
Molecular Formula:C₁₉H₁₇N₅O₆
Molecular Weight:411.374
Hs Code.:
Mol file:122712-57-6.mol

Synonyms:1,2,4-Benzotriazine,L-glutamic acid deriv.

Suppliers and Price of N-(4-(3-oxo-6-amino-2,3-dihydro-1,2,4-benzotriazin-2-yl)benzoyl)glutamic acid

Supply Marketing:

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

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Chemical Property of N-(4-(3-oxo-6-amino-2,3-dihydro-1,2,4-benzotriazin-2-yl)benzoyl)glutamic acid

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：177.50000
Density:1.59g/cm³
LogP:1.38280

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of N-(4-(3-oxo-6-amino-2,3-dihydro-1,2,4-benzotriazin-2-yl)benzoyl)glutamic acid

There total 3 articles about N-(4-(3-oxo-6-amino-2,3-dihydro-1,2,4-benzotriazin-2-yl)benzoyl)glutamic 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: 80.4%

: 122712-56-5
N-(2'-ethoxycarbonylamino-4'-amino-azobenzene-4-carbonyl)-L-glutamic acid

: 122712-57-6
N-<4-(3-oxo-6-amino-2,3-dihydro-1,2,4-benzotriazin-2-yl)benzoyl>-L-glutamic acid

Guidance literature:: With acetic acid; for 3h; Heating;

Reference yield:

: 4271-30-1,532-63-8
N-(4-aminobenzoyl)-L-glutamic acid

: 122712-57-6
N-<4-(3-oxo-6-amino-2,3-dihydro-1,2,4-benzotriazin-2-yl)benzoyl>-L-glutamic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) 37percent HCl, NaNO₂ 2.) CH₃COOH, CH₃COONa / 1.) H₂O, 30 min, 0 deg C - 5 deg C; 2.) H₂O, 24 h, 0 deg C - 5 deg C

2: 80.4 percent / 99percent CH₃COOH / 3 h / Heating

With hydrogenchloride; sodium acetate; acetic acid; sodium nitrite;

Reference yield:

: 122712-58-7
3-Amino-phenylcarbaminsaeureethylester-Hydrochlorid

: 122712-57-6
N-<4-(3-oxo-6-amino-2,3-dihydro-1,2,4-benzotriazin-2-yl)benzoyl>-L-glutamic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) 37percent HCl, NaNO₂ 2.) CH₃COOH, CH₃COONa / 1.) H₂O, 30 min, 0 deg C - 5 deg C; 2.) H₂O, 24 h, 0 deg C - 5 deg C

2: 80.4 percent / 99percent CH₃COOH / 3 h / Heating

With hydrogenchloride; sodium acetate; acetic acid; sodium nitrite;