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重要文件

26235

Sigma-Aldrich

2-(3-氯丙基)-1,3-二噁戊环

≥97.0% (GC)

同義詞:

4-氯丁醛乙烯基乙缩醛

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About This Item

經驗公式(希爾表示法):
C6H11ClO2
CAS號碼:
分子量::
150.60
Beilstein:
1236588
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
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品質等級

化驗

≥97.0% (GC)

形狀

liquid

折射率

n20/D 1.453

bp

93-94 °C/12 mmHg (lit.)

密度

1.142 g/mL at 20 °C (lit.)

官能基

chloro
ether

SMILES 字串

ClCCCC1OCCO1

InChI

1S/C6H11ClO2/c7-3-1-2-6-8-4-5-9-6/h6H,1-5H2

InChI 密鑰

ZBPUNVFDQXYNDY-UHFFFAOYSA-N

應用

2-(3-Chloropropyl)-1,3-dioxolane (2-(3′-chloropropyl)-1,3-dioxolane) is a masked γ-chlorobutyraldehyde and was used for the introduction of 3-(1,3-dioxolan-2-yl)propyl moiety[1][2][3]. It was also used in the synthesis of:
  • (±)-histrionicotoxin and (±)-histrionicotoxin 235A using a two-directional strategy[4]
  • 4-iodobutyraldehyde, 5-iodovaleraldehyde and 5-iodo-2-petanone[5]
  • corresponding phosphonate[6]

其他說明

含掩蔽的 γ-氯丁醛,用于引入 3-(1,3-二氧戊环-2-基)丙基部分[1][2][3];也可用于对应膦酸酯的制备和使用[6]

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

174.2 °F - closed cup

閃點(°C)

79 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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R.E. Abbott et al.
The Journal of Organic Chemistry, 45, 5398-5398 (1980)
C.P. Forbes et al.
Journal of the Chemical Society. Perkin Transactions 1, 2353-2353 (1977)
A Nagy et al.
Proceedings of the National Academy of Sciences of the United States of America, 93(6), 2464-2469 (1996-03-19)
A convenient, high yield conversion of doxorubicin to 3'-deamino-3'-(2''-pyrroline-1''-yl)doxorubicin is described. This daunosamine-modified analog of doxorubicin is 500-1000 times more active in vitro than doxorubicin. The conversion is effected by using a 30-fold excess of 4-iodobutyraldehyde in anhydrous dimethylformamide. The
P.A. Aristoff
The Journal of Organic Chemistry, 50, 1765-1765 (1985)
Two-directional synthesis. Part 1: A short formal synthesis of (?)-histrionicotoxin and (?)-histrionicotoxin 235A.
Stockman RA.
Tetrahedron Letters, 41(47), 9163-9165 (2000)

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