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CAS

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132637-67-3

Pyrrolidine, 1-(phenylselenoxomethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132637-67-3 Structure

  • Basic information

    1. Product Name: Pyrrolidine, 1-(phenylselenoxomethyl)-
    2. Synonyms:
    3. CAS NO:132637-67-3
    4. Molecular Formula: C11H13NSe
    5. Molecular Weight: 238.191
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132637-67-3.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: Pyrrolidine, 1-(phenylselenoxomethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Pyrrolidine, 1-(phenylselenoxomethyl)-(132637-67-3)
    11. EPA Substance Registry System: Pyrrolidine, 1-(phenylselenoxomethyl)-(132637-67-3)

  • 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: 132637-67-3(Hazardous Substances Data)

132637-67-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132637-67-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,6,3 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 132637-67:
(8*1)+(7*3)+(6*2)+(5*6)+(4*3)+(3*7)+(2*6)+(1*7)=123
123 % 10 = 3
So 132637-67-3 is a valid CAS Registry Number.

132637-67-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1'-phenyl-1'-selenoxomethyl)pyrrolidine

1.2 Other means of identification

Product number -
Other names .N-(phenylselenocarbonyl)pyrrolidine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:132637-67-3 SDS

132637-67-3Relevant articles and documents

Tertiary selenoamide compounds are useful superoxide radical scavengers in vitro

Takahashi, Hitoe,Nishina, Atsuyoshi,Kimura, Hirokazu,Motoki, Kenji,Koketsu, Mamoru,Ishihara, Hideharu

, p. 207 - 211 (2007/10/03)

We investigated the scavenging effects of tertiary selenoamide compounds for super oxide radicals using a highly sensitive and quantitative chemiluminescence method. At 333 nM, tertiary selenoamide compounds scavenged 25.8-81.6% of O2-/su

Facile synthesis of N,N-dialkylselenoamides from amides

Koketsu, Mamoru,Okayama, Yoshihiro,Aoki, Hiroshi,Ishihara, Hideharu

, p. 195 - 198 (2007/10/03)

The synthesis of the N,N-dialkylselenoamides from amides was discussed. These selenoamides were chlorinated with oxalyl chloride and then they were allowed to react with LiAlHSeH to afford the corresponding N,N-dialkylamides in moderate to good yields. Af

Reactions of Phosphonate Carbanions with Selenium or Sulfur in the Presence of Amines. Synthesis of Seleno- and Thioamides

Okuma, Kentaro,Ikari, Koumei,Ohta, Hiroshi

, p. 131 - 134 (2007/10/02)

The reaction of phosphonate carbanions with elemental selenium in the presence of amines afforded the corresponding selenoamides in moderate yields.The reaction of these anions with sulfur also gave thioamides.These reactions might proceed through thio- or selenoaldehyde intermediates.

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