Cycloheptene, 96%, stab. with 0.1% BHT
Cycloheptene, 96%, stab. with 0.1% BHT
Cycloheptene, 96%, stab. with 0.1% BHT
Thermo Scientific Chemicals

Cycloheptene, 96%, stab. with 0.1% BHT

CAS: 628-92-2 | C7H12 | 96.173 g/mol
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Quantity:
5 g
25 g
產品號碼 H29062.06
亦稱為 H29062-06
價格 (TWD)
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Quantity:
5 g
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化學識別
CAS628-92-2
IUPAC Namecycloheptene
Molecular FormulaC7H12
InChI KeyZXIJMRYMVAMXQP-UHFFFAOYSA-N
SMILESC1CCC=CCC1
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規格Specification Sheet規格表
Refractive Index1.4550-1.4610 @20?C
FormLiquid
Appearance (Color)Clear colorless
Assay (GC)≥95.0%
Cycloheptene was used in one-pot synthesis of 1,2/3-triols from the allylichydroperoxides catalyzed by zeolite-confined osmium(0) nanoclusters. It is a raw material in organic chemistry and a monomer in polymer synthesis. Copper (1) triflate catalyzes the photodimerization of the simple nonconjugated unstrained olefins, cyclopentene, cyclohexene, and cycloheptene, but not cyclooctene or acyclic olefins.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Cycloheptene was used in one-pot synthesis of 1,2/3-triols from the allylichydroperoxides catalyzed by zeolite-confined osmium(0) nanoclusters. It is a raw material in organic chemistry and a monomer in polymer synthesis. Copper (1) triflate catalyzes the photodimerization of the simple nonconjugated unstrained olefins, cyclopentene, cyclohexene, and cycloheptene, but not cyclooctene or acyclic olefins.

Solubility
Insoluble in water.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, acids. May react exothermically with reducing agents to release hydrogen gas.
RUO – Research Use Only

General References:

  1. Göksu H, et al. J. One-pot synthesis of 1, 2/3-triols from the allylic hydroperoxides catalyzed by zeolite-confined osmium (0) nanoclusters. Mol. Catal. A: Chem.. 2013, 378 142-147.
  2. Robert G. Salomon,; Kirsten Folting,; William E. Streib,; Jay K. Kochi. Copper(I) catalysis in photocycloadditions. II. Cyclopentene, cyclohexene, and cycloheptene. J. Am. Chem. Soc. 1974, 96(4),1145-1152.