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38183-12-9 分子结构
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4'-phenyl-3H,3'H-spiro[2-benzofuran-1,2'-furan]-3,3'-dione

ChemBase编号:105940
分子式:C17H10O4
平均质量:278.2589
单一同位素质量:278.0579088
SMILES和InChIs

SMILES:
O=C1OC2(OC=C(C2=O)c2ccccc2)c2ccccc12
Canonical SMILES:
O=C1OC2(c3c1cccc3)OC=C(C2=O)c1ccccc1
InChI:
InChI=1S/C17H10O4/c18-15-13(11-6-2-1-3-7-11)10-20-17(15)14-9-5-4-8-12(14)16(19)21-17/h1-10H
InChIKey:
ZFKJVJIDPQDDFY-UHFFFAOYSA-N

引用这个纪录

CBID:105940 http://www.chembase.cn/molecule-105940.html

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名称和登记号

名称和登记号

名称 登记号
IUPAC标准名
4'-phenyl-3H,3'H-spiro[2-benzofuran-1,2'-furan]-3,3'-dione
IUPAC传统名
fluorescamine
别名
荧光胺
4-Phenylspiro[furan-2(3H)-1'-(3'-H)-Isobenzofuran]-3,3'-dione
FLUORESCAMINE
4-Phenylspiro-[furan-2(3H),1-phthalan]-3,3′-dione
Fluorescamine
Fluram
CAS号
38183-12-9
EC号
253-814-5
MDL号
MFCD00005928
Beilstein号
921143
默克索引号
144158
PubChem SID
24894984
162092857
PubChem CID
37927
维基百科标题
Fluorescamine

理论计算性质

理论计算性质

JChem
质子受体 质子供体
LogD (pH = 5.5) 3.975393  LogD (pH = 7.4) 3.975393 
Log P 3.975393  摩尔折射率 75.1287 cm3
极化性 28.987541 Å3 极化表面积 52.6 Å2
可自由旋转的化学键 里宾斯基五规则 true 

分子性质

分子性质

理化性质 安全信息 产品相关信息 生物活性(PubChem)
溶解度
acetone: soluble50 mg/mL expand 查看数据来源
外观
off-white to yellow powder expand 查看数据来源
Powder expand 查看数据来源
熔点
148-158°C expand 查看数据来源
153-157 °C(lit.) expand 查看数据来源
153–157 °C expand 查看数据来源
155-158°C expand 查看数据来源
紫外吸收波长
λmax 306 nm expand 查看数据来源
保存条件
Room Temperature (15-30°C) expand 查看数据来源
MSDS下载
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源
德国WGK号
3 expand 查看数据来源
TSCA收录
expand 查看数据来源
个人保护装置
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter expand 查看数据来源
纯度
≥98% (TLC) expand 查看数据来源
≥98.0% expand 查看数据来源
98% expand 查看数据来源
质检报告
下载链接 expand 查看数据来源
产品质量级别
PREMIUM expand 查看数据来源
Empirical Formula (Hill Notation)
C17H10O4 expand 查看数据来源

详细说明

详细说明

MP Biomedicals MP Biomedicals Wikipedia Wikipedia Sigma Aldrich Sigma Aldrich
MP Biomedicals -  02195183 external link
Off-white to yellow powder.
Reagent for fluorescent assay of amino acids, peptides, proteins and other primary amines.1,2. Also used for fluorometric assays of some proteolytic enzymes.3
Sigma Aldrich -  F9015 external link
Application
Non-fluorescent reagent that reacts readily under mild conditions with primary amines in amino acids and peptides to form stable, highly fluorescent compounds.1,2 Low background due to hydrolysis. Useful for the fluorometric assay of amino acids, protein, and proteolytic enzymes.3 Effectively blocks newly generated amino termini in protein sequence analyses.
包装
1 g in glass bottle
100, 250 mg in glass bottle
Sigma Aldrich -  201650 external link
Application
Non-fluorescent reagent that reacts readily under mild conditions with primary amines in amino acids and peptides to form stable, highly fluorescent compounds.1,2 Low background due to hydrolysis. Useful for the fluorometric assay of amino acids, protein, and proteolytic enzymes.3 Effectively blocks newly generated amino termini in protein sequence analyses.
包装
100 mg in glass bottle
Sigma Aldrich -  11-0398 external link
Application
Non-fluorescent reagent that reacts readily under mild conditions with primary amines in amino acids and peptides to form stable, highly fluorescent compounds.1,2 Low background due to hydrolysis. Useful for the fluorometric assay of amino acids, protein, and proteolytic enzymes.3 Effectively blocks newly generated amino termini in protein sequence analyses.
Suitability
for HPLC

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • Weigele, M., et al., J. Am. Chem. Soc. , 94 : 5927 (1972).
  • Udenfriend, S., et al., Science , 178 : 871 (1972).
  • Sogowa, K. and Takahashi, K.J., Biochem. (Tokyo) , 83 : 1783 (1978).
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专利

专利

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互联网资源

互联网资源

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