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172685-27-7

3-Chloro-2-pyrrolidino-5-(triisopropylsiloxy)cyclohexene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 172685-27-7 Structure

  • Basic information

    1. Product Name: 3-Chloro-2-pyrrolidino-5-(triisopropylsiloxy)cyclohexene
    2. Synonyms: 3-Chloro-2-pyrrolidino-5-(triisopropylsiloxy)cyclohexene
    3. CAS NO:172685-27-7
    4. Molecular Formula:
    5. Molecular Weight: 358.039
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 172685-27-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-Chloro-2-pyrrolidino-5-(triisopropylsiloxy)cyclohexene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Chloro-2-pyrrolidino-5-(triisopropylsiloxy)cyclohexene(172685-27-7)
    11. EPA Substance Registry System: 3-Chloro-2-pyrrolidino-5-(triisopropylsiloxy)cyclohexene(172685-27-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 172685-27-7(Hazardous Substances Data)

172685-27-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 172685-27-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,6,8 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 172685-27:
(8*1)+(7*7)+(6*2)+(5*6)+(4*8)+(3*5)+(2*2)+(1*7)=157
157 % 10 = 7
So 172685-27-7 is a valid CAS Registry Number.

172685-27-7Upstream product

172685-27-7Downstream Products

172685-27-7Relevant articles and documents

Fragmentation of Alkoxy Radicals and Oxidative Elimination of Alicyclic Iodides

Lee, Jinhwa,Oh, Jonghoon,Jin, Shu-juan,Choi, Jong-Ryoo,Atwood, Jerry L.,Cha, Jin Kun

, p. 6955 - 6964 (1994)

The azaallyl cation-mediated cycloaddition with spirohepta-4,6-diene by the procedure of Schmid provides the tricyclic cycloadducts of general type 3.The keto bridge of the cycloadducts 17c, 21, and 22 has been cleaved by PhI(OAc)2-I2 (Suarez cleavage), which involves β-fragmentation of an alkoxy radical, to furnish iodo lactones 19, 32, and 30a,b, respectively.Subsequent oxidation of these alkyl iodides has been investigated to develop a new synthetic route for bridgehead olefins (i.e., 33) of medium-sized carbocycles.

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