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Merck

H53704

Sigma-Aldrich

N-羟基邻苯二甲酰亚胺

97%, for peptide synthesis

别名:

2-Hydroxy-1H-isoindole-1,3(2H)-dione, 2-Hydroxyisoindole-1,3-dione, 2-Hydroxyphthalimide

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About This Item

经验公式(希尔记法):
C8H5NO3
CAS号:
分子量:
163.13
Beilstein:
131208
EC 号:
MDL编号:
UNSPSC代码:
12352005
PubChem化学物质编号:
NACRES:
NA.22

产品名称

N-羟基邻苯二甲酰亚胺, 97%

质量水平

方案

97%

表单

crystalline

反应适用性

reaction type: Addition Reactions

mp

233 °C (dec.) (lit.)

应用

peptide synthesis

SMILES字符串

ON1C(=O)c2ccccc2C1=O

InChI

1S/C8H5NO3/c10-7-5-3-1-2-4-6(5)8(11)9(7)12/h1-4,12H

InChI key

CFMZSMGAMPBRBE-UHFFFAOYSA-N

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应用

制备胺核苷,以用于偶联反应生成非阴离子反义寡聚核苷。

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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其他客户在看

Tetrahedron Letters, 33, 2645-2645 (1992)
H M Petrassi et al.
Organic letters, 3(1), 139-142 (2001-06-30)
[figure: see text] A novel route to aryloxyamines via the copper-mediated cross-coupling of N-hydroxyphthalimide and phenylboronic acids is reported. The reaction is mediated by selected copper(I) and (II) salts in the presence of pyridine and is tolerant of several functional
[Hydroxyphthalimide induced medicamentosa-like dermatitis in five patients].
Jian-fang Zou et al.
Zhonghua lao dong wei sheng zhi ye bing za zhi = Zhonghua laodong weisheng zhiyebing zazhi = Chinese journal of industrial hygiene and occupational diseases, 24(10), 625-625 (2006-11-14)
James M Takacs et al.
Organic letters, 5(20), 3595-3598 (2003-09-26)
[reaction: see text] Screening combinations of five catalyst precursors with 13 phosphorus ligands identified cyclization catalysts that favor carbocyclization-trapping with N-hydroxyphthalimide over a competing cycloisomerization mode.
M H Lang et al.
Dermatosen in Beruf und Umwelt. Occupation and environment, 35(6), 212-213 (1987-11-01)
We report a case of a female laboratory worker in the chemical industry who acquired contact allergy to dicyclohexylcarbodiimide and N-hydroxyphthalimide. Both substances are used in the chemical synthesis of peptides. So far there have only been a few reports

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