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188611

3-[2-(二乙氨基)乙基]-7-羟基-4-甲基香豆素盐酸盐

Name: 3-[2-(二乙氨基)乙基]-7-羟基-4-甲基香豆素 盐酸盐
Brand: ALDRICH

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About This Item

經驗公式（希爾表示法）:

C₁₆H₂₁NO₃ · HCl

CAS號碼:

15776-59-7

分子量：:

311.80

EC號碼:

239-872-4

MDL號碼:

MFCD00006855

分類程式碼代碼:

12352100

PubChem物質ID:

24851169

NACRES:

NA.22

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Sigma-Aldrich

175633

硅油

Sigma-Aldrich

273619

1′,3′-二氢-1′3′,3′-三甲基-6-硝基螺[2H-1-苯并吡喃-2,2′-(2H)-吲哚]

Sigma-Aldrich

440140

(3-氨基丙基)三乙氧基硅烷

Sigma-Aldrich

331406

顺-二氯双(三乙基膦)铂(II)

Sigma-Aldrich

479519

铂(0)-1,3-二乙烯-1,1,3,3-四甲基二硅氧烷络合物溶液

Sigma-Aldrich

433012

聚(二甲基硅氧烷)，乙烯基封端

Sigma-Aldrich

402737

酞菁镁

Sigma-Aldrich

8.20760

di-Manganese decacarbonyl

Sigma-Aldrich

S5130

气相二氧化硅

Sigma-Aldrich

C9322

过氧化氢酶来源于牛肝脏

形狀

solid

mp

284-287 °C (dec.) (lit.)

官能基

amine
ester

SMILES 字串

Cl[H].CCN(CC)CCC1=C(C)c2ccc(O)cc2OC1=O

InChI

1S/C16H21NO3.ClH/c1-4-17(5-2)9-8-14-11(3)13-7-6-12(18)10-15(13)20-16(14)19;/h6-7,10,18H,4-5,8-9H2,1-3H3;1H

InChI 密鑰

RLJNKMCFVQMDFR-UHFFFAOYSA-N

應用

3-[2-(Diethylamino)ethyl]-7-hydroxy-4-methylcoumarin hydrochloride was used in the synthesis of:

novel metal-free and zinc phthalocyanines with four 3-[(2-diethylamino)ethyl]-7-oxo-4-methylcoumarin dye groups via cyclotetramerization[1]
3-(2-diethylaminoethyl)-4-methyl-7-substituted coumarins, having antifungal activities against Botrytis cinerea[2]

象形圖

GHS07

訊號詞

Warning

危險聲明

H315,H319,H335

防範說明

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

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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分析證明 (COA)

Lot/Batch Number

08605AU

03406HN

01814BI

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Synthesis and characterization of novel phthalocyanines bearing quaternizable coumarin.

Cakici H, et al.

Polyhedron, 27(18), 3625-3630 (2008)

Synthesis and in vitro evaluation of novel 1, 2, 4-triazole derivatives as antifungal agents.

Kokil GR, et al.

Letters in Drug Design & Discovery, 7(1), 46-49 (2010)

Induction via Functional Protein Stabilization of Hepatic Cytochromes P450 upon gp78/Autocrine Motility Factor Receptor (AMFR) Ubiquitin E3-Ligase Genetic Ablation in Mice: Therapeutic and Toxicological Relevance.

Doyoung Kwon et al.

Molecular pharmacology, 96(5), 641-654 (2019-09-08)

The hepatic endoplasmic reticulum (ER)-anchored monotopic proteins, cytochromes P450 (P450s), are enzymes that metabolize endobiotics (physiologically active steroids and fatty acids), as well as xenobiotics including therapeutic/chemotherapeutic drugs, nutrients, carcinogens, and toxins. Alterations of hepatic P450 content through synthesis, inactivation

Novel Coumarin Substituted Water Soluble Cyclophosphazenes as "Turn-Off" Type Fluorescence Chemosensors for Detection of Fe(3+) ions in Aqueous Media.

Gönül Yenilmez Çiftçi et al.

Journal of fluorescence, 25(6), 1819-1830 (2015-10-01)

In the present work, 3-[2-(diethylamino)ethyl]-7-oxy-4-methylcoumarin substituted cyclotriphosphazene (4) and cyclotetraphosphazene (5) derivatives were synthesized by the reactions of hexachlorocyclotriphosphazene (1) or octachlorocyclotetraphosphazene (2) with 3-[2-(diethylamino)ethyl]-7-hydroxy-4-methylcoumarin (3) for the first time. The quaternized cationic (6 and 7) and zwitterionic (8 and

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