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Merck
CN

419591

3-丁烯基溴化镁 溶液

0.5 M in THF

别名:

1-(溴化镁)-3-丁烯, 1-丁烯-4-基溴化镁, 3-丁烯基溴化镁, 溴-3-丁烯-1-基镁

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关于此项目

线性分子式:
H2C=CHCH2CH2MgBr
化学文摘社编号:
分子量:
159.31
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
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产品名称

3-丁烯基溴化镁 溶液, 0.5 M in THF

InChI

1S/C4H7.BrH.Mg/c1-3-4-2;;/h3H,1-2,4H2;1H;/q;;+1/p-1

SMILES string

Br[Mg]CCC=C

InChI key

SMLLHQBZPPSOSR-UHFFFAOYSA-M

reaction suitability

reaction type: Grignard Reaction

concentration

0.5 M in THF

bp

65 °C

density

0.937 g/mL at 25 °C

functional group

allyl

Quality Level

Application

可参与钌催化剂协助的环化反应的合成结构单元。
用于由 L-酒石酸合成 (–)-muricatacin 的非对映选择性关键步骤。

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 3 - Water-react 1

target_organs

Central nervous system, Respiratory system

supp_hazards

存储类别

4.3 - Hazardous materials which set free flammable gases upon contact with water

wgk

WGK 3

flash_point_f

-22.0 °F - closed cup

flash_point_c

-30 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves

法规信息

危险化学品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Aleksandar Ivkovic et al.
Organic letters, 6(8), 1221-1224 (2004-04-09)
The combination of alkene metathesis and beta-fragmentation offers an efficient entry into (Z)-configured medium-ring cycloalkenes. The versatility of this method is demonstrated by the total synthesis of Periplanone C, a semiochemical of Periplaneta americana. [reaction: see text]
Tetrahedron Asymmetry, 17, 2465-2465 (2006)
Jehrod B Brenneman et al.
Organic letters, 6(8), 1329-1331 (2004-04-09)
A concise synthesis of the potent nAChR agonist (+)-anatoxin-a (1) has been completed in a series of only nine chemical operations and 27% overall yield from commercially available D-methyl pyroglutamate (4). The synthesis features a novel procedure for the diastereoselective
Toshio Honda et al.
Organic letters, 6(1), 87-89 (2004-01-03)
[reaction: see text] A diastereoselective total synthesis of securinine in optically pure form was achieved by employing ring-closing metathesis of the corresponding dienyne compound as a key step.

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