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Key Documents

T14400

Sigma-Aldrich

四氢吡喃

ReagentPlus®, 99%

同義詞:

氧己环

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About This Item

經驗公式(希爾表示法):
C5H10O
CAS號碼:
分子量::
86.13
Beilstein:
102436
EC號碼:
MDL號碼:
分類程式碼代碼:
12190000

蒸汽密度

3 (vs air)

產品線

ReagentPlus®

化驗

99%

折射率

n20/D 1.42 (lit.)

bp

88 °C (lit.)

mp

−45 °C (lit.)

密度

0.881 g/mL at 25 °C (lit.)

SMILES 字串

C1CCOCC1

InChI

1S/C5H10O/c1-2-4-6-5-3-1/h1-5H2

InChI 密鑰

DHXVGJBLRPWPCS-UHFFFAOYSA-N

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法律資訊

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

取代透過

產品號碼
描述
訂價

象形圖

Flame

訊號詞

Danger

危險聲明

危險分類

Flam. Liq. 2

安全危害

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

3.2 °F - closed cup

閃點(°C)

-16 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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分析證明 (COA)

Lot/Batch Number

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Yantao Wei et al.
Retina (Philadelphia, Pa.), 35(8), 1631-1639 (2015-07-28)
To evaluate the surgical approach of pars plana vitrectomy combined with 360° retinotomy and silicon oil tamponade in the treatment of patients with large subretinal hemorrhage. Prospective, nonrandomized, and noncomparative case series study. Consecutive patients with breakthrough vitreous hemorrhage and
Paul A Clarke et al.
Organic & biomolecular chemistry, 13(16), 4743-4750 (2015-03-26)
The Maitland-Japp reaction has been extended to the synthesis of highly functionalised dihydropyran-4-ones. These dihydropyran-4-ones can in turn be converted stereoselectively into tetrahydropyran-4-ones with tertiary and quaternary stereocentres via the one-pot addition of hydride or carbon nucleophiles and trapping with
B V Subba Reddy et al.
Organic & biomolecular chemistry, 13(24), 6737-6741 (2015-05-23)
A domino reaction has been developed for the synthesis of oxygen bridged bicyclic ethers through the coupling of 4-(2-hydroxyethyl)cyclohex-3-enols with aldehydes in the presence of 10 mol% of molecular iodine in dichloromethane at 25 °C. This method is highly diastereoselective
Francesco Paolo Di Nicola et al.
Dalton transactions (Cambridge, England : 2003), 44(28), 12653-12659 (2015-06-17)
Distinct batches of orange (1a-e) and green crystals (2a-e) were isolated from the reactions of MoCl5 with tetrahydropyran (thp), respectively at room temperature (in CH2Cl2) and at ca. 80 °C (in ClCH2CH2Cl). Crystals 2a-e are isomorphous to 1a-e and the

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