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Merck
CN

79850

N-邻苯二甲酰甘氨酸

puriss., ≥99.0% (T)

别名:

1,3-二氧-2-异吲哚啉乙酸, 邻苯二甲酰甘氨酸

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关于此项目

经验公式(希尔记法):
C10H7NO4
化学文摘社编号:
分子量:
205.17
UNSPSC Code:
12352200
PubChem Substance ID:
eCl@ss:
32160406
EC Number:
225-177-3
Beilstein/REAXYS Number:
184174
MDL number:
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grade

puriss.

assay

≥99.0% (T)

ign. residue

≤0.05%

mp

193-196 °C

application(s)

peptide synthesis

SMILES string

OC(=O)CN1C(=O)c2ccccc2C1=O

InChI

1S/C10H7NO4/c12-8(13)5-11-9(14)6-3-1-2-4-7(6)10(11)15/h1-4H,5H2,(H,12,13)

InChI key

WQINSVOOIJDOLJ-UHFFFAOYSA-N

Other Notes

受保护的甘氨酸。这种酸的氯化物被用于 (2+2) 烯酮-亚胺环加成反应


pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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C. Hubschwerlen et al.
Organic Syntheses, 72, 14-14 (1995)
Julija Matijević-Sosa et al.
Acta pharmaceutica (Zagreb, Croatia), 58(2), 231-236 (2008-06-03)
The aim of this study was to investigate the activity of N-phthaloyl-glycine-hydroxamic acid (Phth-Gly-HA) as a new iron chelator in vivo to be used in iron overload diseases. After intraperitoneal application of Phth-Gly-HA to male rats (1 mg kg(-1) body
O abu Salach et al.
Pharmaceutical research, 11(10), 1429-1434 (1994-10-01)
Glycine, in addition to GABA, is one of the most important neurotransmitter amino acids. The described structure pharmacokinetic pharmacodynamic relationships (SPPR) study explored the possibility of utilizing phthaloyl derivatives of glycine as new antiepileptics. This was carried out by investigating