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335312

2-戊炔-1-醇

Name: 2-戊炔-1-醇
Brand: ALDRICH
Price: 1798.78 CNY

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250 G

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250 G

¥1,798.78

1 KG

¥5,444.19

About This Item

线性分子式:

C₂H₅C≡CCH₂OH

CAS号:

6261-22-9

分子量:

84.12

Beilstein:

1734007

EC 号:

228-411-2

MDL编号:

MFCD00040915

UNSPSC代码:

12352100

PubChem化学物质编号:

24860304

NACRES:

NA.22

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此商品	R8881	T5428	D6665
D1054 二氢罗丹明123	R8881 罗丹明 B 异硫氰酸酯-葡聚糖	T5428 四甲基罗丹明甲酯高氯酸盐	D6665 2′,7′-二氯荧光素
color pink	color light pink to red, very dark purple	color dark green	color -
solubility DMSO: >5 mg/mL	solubility water: 10 mg/mL, clear, pink	solubility methanol: 5 mg/mL, clear	solubility ethanol: 25 mg/mL
application(s) diagnostic assay manufacturing hematology histology	application(s) diagnostic assay manufacturing hematology histology	application(s) diagnostic assay manufacturing hematology histology	application(s) diagnostic assay manufacturing hematology histology
form powder	form powder	form powder	form powder
Quality Level 200	Quality Level 200	Quality Level 200	Quality Level 200
assay ≥95%	assay -	assay ≥95%	assay ~90% (TLC)

应用

2-Pentyn-1-ol was employed as starting reagent for the synthesis of (-)-muricatacin.[1] It was also used in the preparation of (2Z)-3-tributylstannyl-2-penten-1-ol.[2]

象形图

GHS02,GHS07

警示用语：

Warning

危险声明

H226,H315,H319,H335

预防措施声明

P210 - P302 + P352 - P305 + P351 + P338

危险分类

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

靶器官

Respiratory system

储存分类代码

3 - Flammable liquids

WGK

WGK 3

闪点(°F)

136.4 °F - closed cup

闪点(°C)

58 °C - closed cup

个人防护装备

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Synthesis of 9Z-9-substituted retinoic acids by palladium catalyzed coupling reaction of a vinyl triflate with alkenyl stannanes.

A Wada et al.

Chemical & pharmaceutical bulletin, 48(9), 1391-1394 (2000-09-19)

Palladium catalyzed cross coupling reactions of a vinyl triflate intermediate and various alkenyl stannanes afforded trisubstituted Z-olefins stereoselectively in high yields. These olefins were then converted to the corresponding 9Z-retinoic acids via Horner-Emmons reaction and subsequent basic hydrolysis in excellent

Synthesis of (-)-muricatacin.

H Makabe et al.

Bioscience, biotechnology, and biochemistry, 57(6), 1028-1029 (1993-06-01)

The synthesis of (-)-muricatacin starting from 1-bromododecane and 2-pentyn-1-ol is described. 2-Pentadecyn-1-ol (4), which was prepared from 1-bromododecane (2) and 2-pentyn-1-ol (3), was converted to epoxy alcohol 6 through a two-step reaction sequence, 6 being successively submitted to tosylation, iodination

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2-戊炔-1-醇

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预防措施声明

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WGK

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