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Merck

209880

Sigma-Aldrich

5-苯基邻茴香胺

≥98%

别名:

2-甲氧基-5-苯基苯胺

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About This Item

线性分子式:
C6H5C6H3(OCH3)NH2
CAS号:
分子量:
199.25
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
形狀:
powder
化驗:
≥98%

品質等級

化驗

≥98%

形狀

powder

mp

82-83 °C (lit.)

官能基

phenyl

SMILES 字串

COc1ccc(cc1N)-c2ccccc2

InChI

1S/C13H13NO/c1-15-13-8-7-11(9-12(13)14)10-5-3-2-4-6-10/h2-9H,14H2,1H3

InChI 密鑰

DTYBRSLINXBXMP-UHFFFAOYSA-N

一般說明

5-Phenyl-o-anisidine is a promising monomer for polyanilines studies. X-ray Diffraction and DFT studies of 5-phenyl-o-anisidine (2-methoxy-5-phenylaniline) have been reported.

應用

5-Phenyl-o-anisidine (2-Methoxy-5-phenylaniline) was used in the synthesis of 2,4-diamino-5-methyl-6-substituted-pyrido[2,3-d]pyrimidines.

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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分析证书(COA)

Lot/Batch Number

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A Gangjee et al.
Journal of medicinal chemistry, 40(4), 479-485 (1997-02-14)
Nine novel 2,4-diamino-5-methyl-6-substituted-pyrido[2,3-d]pyrimidines, 2-10, were synthesized as potential inhibitors of Pneumocystis carinii dihydrofolate reductase (pcDHFR) and Toxoplasma gondii dihydrofolate reductase (tgDHFR). Compounds 2-5 were designed as conformationally restricted analogues of trimetrexate (TMQ), in which rotation around tau 3 was constrained
X-ray Diffraction and DFT Studies of 2-Methoxy-5-phenylaniline.
Marques AT, et al.
Journal of Chemical Crystallography, 38(4), 295-299 (2008)

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