GLUTAMATE CAGED

Base Information

Chemical Name:GLUTAMATE CAGED
CAS No.:239135-34-3
Molecular Formula:C16H19 N3 O7
Molecular Weight:365.343
Hs Code.:2922509090
Mol file:239135-34-3.mol

Synonyms:caged glutamate;Caged Glutamate hydrate, (S)-Methyl 1-[5-(4-amino-4-carboxybutanoyl)]-7-nitroindoline-5-acetate hydrate;Glutamate, Caged hydrate

Suppliers and Price of GLUTAMATE CAGED

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

Sigma-Aldrich
Glutamate, Caged hydrate powder
50mg
$ 2260.00

Sigma-Aldrich
Glutamate, Caged hydrate powder
10mg
$ 701.00

American Custom Chemicals Corporation
GLUTAMATE, CAGED HYDRATE 95.00%
50MG
$ 2674.12

American Custom Chemicals Corporation
GLUTAMATE, CAGED HYDRATE 95.00%
10MG
$ 1139.38

Total 2 raw suppliers

Chemical Property of GLUTAMATE CAGED

Chemical Property:

PSA：155.75000
LogP:1.68000
Storage Temp.:−20°C
Solubility.:H2O: >10 mg/mL

Purity/Quality:

97% ^*data from raw suppliers

Glutamate, Caged hydrate powder ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Uses Glutamate, Caged hydrate has been used: as a supplement in neurobasal medium for primary culture of mouse cortical neuronsas a supplemental glutamate in laboratory-prepared food (LF)as a component of slicing solution used for perfusing the animal in mouse brain-slice experiments

Technology Process of GLUTAMATE CAGED

There total 5 articles about GLUTAMATE CAGED 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: 81.0%

: 239135-31-0
methyl 1-(S)-{[(4-tert-butoxycarbonyl)-4-(tert-butoxycarbonylamino)]butanoyl}indoline-5-acetate

: 1-[S-(4-amino-4-carboxybutanoyl)]-7-nitroindoline-5-acetic acid

: 239135-34-3
methyl 1-[S-(4-amino-4-carboxybutanoyl)]-7-nitroindoline-5-acetate

Guidance literature:: With sodium nitrate; trifluoroacetic acid; at 20 ℃; for 4h;

Reference yield:

: 16078-35-6
1-(1-acetylindolin-5-yl)ethanone

: 239135-34-3
methyl 1-[S-(4-amino-4-carboxybutanoyl)]-7-nitroindoline-5-acetate

Guidance literature:: Multi-step reaction with 4 steps

1: Tl(NO₃)3, HClO₄

2: aq. HCl / methanol

3: EDC, DMAP

4: NaNO₃, Tfa

With hydrogenchloride; dmap; sodium nitrate; perchloric acid; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; trifluoroacetic acid; thallium(III) nitrate; In methanol;
DOI:10.1021/ja990931e

Reference yield:

: 81709-42-4
1-acetyl-2,3-dihydro-1H-indole-5-acetic acid, methyl ester

: 239135-34-3
methyl 1-[S-(4-amino-4-carboxybutanoyl)]-7-nitroindoline-5-acetate

Guidance literature:: Multi-step reaction with 3 steps

1: aq. HCl / methanol

2: EDC, DMAP

3: NaNO₃, Tfa

With hydrogenchloride; dmap; sodium nitrate; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; trifluoroacetic acid; In methanol;
DOI:10.1021/ja990931e