Welcome to LookChem.com Sign In|Join Free

CAS

  • or

132883-44-4

Post Buying Request

132883-44-4 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

132883-44-4 Usage

Chemical Properties

Colorless to light yellow liqui

Uses

(S)-(?)-3-(Dimethylamino)pyrrolidine can be used as a reactant in the syntheses of oxadiazolylthiazole and xanthone derivatives of biological importance.

Check Digit Verification of cas no

The CAS Registry Mumber 132883-44-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,8,8 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 132883-44:
(8*1)+(7*3)+(6*2)+(5*8)+(4*8)+(3*3)+(2*4)+(1*4)=134
134 % 10 = 4
So 132883-44-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H14N2/c1-8(2)6-3-4-7-5-6/h6-7H,3-5H2,1-2H3/t6-/m0/s1

132883-44-4 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (D2193)  (3S)-(-)-3-(Dimethylamino)pyrrolidine  >98.0%(GC)

  • 132883-44-4

  • 1g

  • 1,140.00CNY

  • Detail
  • TCI America

  • (D2193)  (3S)-(-)-3-(Dimethylamino)pyrrolidine  >98.0%(GC)

  • 132883-44-4

  • 5g

  • 3,830.00CNY

  • Detail
  • Aldrich

  • (656704)  (S)-(−)-3-(Dimethylamino)pyrrolidine  97%

  • 132883-44-4

  • 656704-1G

  • 1,881.36CNY

  • Detail

132883-44-4SDS

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 (3S)-(-)-3-(Dimethylamino)Pyrrolidine

1.2 Other means of identification

Product number -
Other names (3S)-(-)-3-(DiMethylaMino)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:132883-44-4 SDS

132883-44-4Upstream product

132883-44-4Relevant articles and documents

FUSED-RING OR TRICYCLIC ARYL PYRIMIDINE COMPOUND USED AS KINASE INHIBITOR

-

Paragraph 0131; 0132, (2018/03/25)

Disclosed is a fused-ring or tricyclic aryl pyrimidine compound used as a mutation selectivity EGFR inhibitor. Specifically, disclosed is a compound represented by formula (I) and used as an EGFR inhibitor or a pharmaceutically acceptable salt thereof.

Dibenzo-epines: Effect of the basic side-chain on neuroleptic activity

Burki,Fischer,Hunziker,et al.

, p. 479 - 485 (2007/10/05)

Structure-activity relationships in a series of dibenzo[b,f][1,4]thiazepines and -oxazepines and dibenzo[b,e][1,4]diazepines having different basic substituents in the 11-position were studied with reference to their neuroleptic activity. A high degree of structure-specificity was found for the piperazinyl moiety as well as for the distances between the distal nitrogen atom of this group and the tricyclic ring system, which distances are probably of importance for receptor binding. It was shown that the N-oxides of the neuroleptic agents clotiapine, loxapine and clozapine were inactive in in vitro binding tests involving central dopaminergic receptors, and it is very likely therefore that the in vivo activity of these N-oxides in the rat is due to their enzymatic reduction to the active parent compounds. All derivatives having a basic side-chain other than N-alkylpiperazinyl were inactive neuroleptically, with the exception of the N-methyl-4-piperidyl derivative which showed relatively weak effects.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 132883-44-4