ChemicalBook > Product Catalog > Organic Chemistry > Hydrocarbons and derivatives > Hydrocarbon halides > DIBENZOSUBERYL CHLORIDE
DIBENZOSUBERYL CHLORIDE
DIBENZOSUBERYL CHLORIDE Basic information
- Product Name:
- DIBENZOSUBERYL CHLORIDE
- Synonyms:
-
- d)cycloheptene,10,11-dihydro-5-chloro-5h-dibenzo(
- 5-CHLORO-10,11-DIHYDRO-5H-DIBENZO[A,D]CYCLOHEPTENE
- 5-CHLORODIBENZOSUBERANE
- DIBENZOSUBERYL CHLORIDE
- 5-Chlorodibenzosuberane~5-Chloro-10,11-dihydro-5H-dibenzo[a,d]cycloheptene
- 5-CHLOROBENZOSUBERANE
- 10,11-Dihydro-5-chloro-5H-dibenzo[a,d]cycloheptene
- 5-Chloro-2,3:6,7-dibenzosuberane
- CAS:
- 1210-33-9
- MF:
- C15H13Cl
- MW:
- 228.72
- EINECS:
- 214-910-2
- Product Categories:
-
- Alkyl
- Building Blocks
- Protection & Derivatization Reagents (for Synthesis)
- Chemical Synthesis
- Halogenated Hydrocarbons
- Organic Building Blocks
- Synthetic Organic Chemistry
- Mol File:
- 1210-33-9.mol
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DIBENZOSUBERYL CHLORIDE Chemical Properties
- Melting point:
- 106-107 °C (lit.)
- Boiling point:
- 321.7±31.0 °C(Predicted)
- Density
- 1.19±0.1 g/cm3(Predicted)
- storage temp.
- Inert atmosphere,Room Temperature
- solubility
- Chloroform (Slightly), Ethyl Acetate (Slightly)
- form
- Solid
- color
- Off-White to Pale Beige
- Sensitive
- Moisture Sensitive
- BRN
- 612280
- Stability:
- Light Sensitive
- InChIKey
- QPERNSDCEUTOTE-UHFFFAOYSA-N
- CAS DataBase Reference
- 1210-33-9(CAS DataBase Reference)
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Safety Information
- Risk Statements
- 34
- Safety Statements
- 26-36/37/39-45
- RIDADR
- 3261
- WGK Germany
- 3
- RTECS
- HO8302000
- HazardClass
- 8
- PackingGroup
- II
- HS Code
- 29039930
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
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DIBENZOSUBERYL CHLORIDE Usage And Synthesis
Uses
Reagent for introduction of the 5-dibenzosuberyl moiety as a modulator for anticancer drugs.1
Uses
Dibenzosuberyl Chloride is used in the synthesis of atypical tricyclic antidepressant as well as dibenzosuberyl-substituted tropines as ligands for acetylcholine-binding protein. Dibenzosuberyl Chloride is also used in the preparation of amino protecting group for solid phase peptide synthesis.
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