Welcome to LookChem.com Sign In|Join Free

CAS

  • or

503-01-5

Post Buying Request

503-01-5 Suppliers

Recommended suppliersmore

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

503-01-5 Usage

Originator

Octinum,Knoll,US,1948

Uses

Different sources of media describe the Uses of 503-01-5 differently. You can refer to the following data:
1. ctin (Knoll).
2. 6-Methylamino-2-methylheptene is an intermediate for the synthesis of Isometheptene Maleate (I821325), which belongs to a group of sympathomimetic amine and shows very little antihypertensive activity. Isometheptene Maleate is used as an antispasmodic drug.

Manufacturing Process

Methyl heptenone dissolved in 75% alcohol is reduced with activated aluminum in the presence of methylamine to give isometheptene.

Therapeutic Function

Muscle relaxant

Check Digit Verification of cas no

The CAS Registry Mumber 503-01-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,0 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 503-01:
(5*5)+(4*0)+(3*3)+(2*0)+(1*1)=35
35 % 10 = 5
So 503-01-5 is a valid CAS Registry Number.

503-01-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N,6-dimethylhept-5-en-2-amine

1.2 Other means of identification

Product number -
Other names Methylisooctenylamine

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:503-01-5 SDS

503-01-5Downstream Products

503-01-5Relevant articles and documents

Enabling New Modes of Reactivity via Constrictive Binding in a Supramolecular-Assembly-Catalyzed Aza-Prins Cyclization

Kaphan, David M.,Toste, F. Dean,Bergman, Robert G.,Raymond, Kenneth N.

supporting information, p. 9202 - 9205 (2015/08/18)

Supramolecular assembly 1 catalyzes a bimolecular aza-Prins cyclization featuring an unexpected transannular 1,5-hydride transfer. This reaction pathway, which is promoted by constrictive binding within the supramolecular cavity of 1, is kinetically disfavored in the absence of 1, as evidenced by the orthogonal reactivity observed in bulk solution. Mechanistic investigation through kinetic analysis and isotopic labeling studies indicates that the rate-limiting step of the transformation is the encapsulation of a transient iminium ion and supports the proposed 1,5-hydride transfer mechanism. This represents a rare example of such an extreme divergence of product selectivity observed within a catalytic metal-ligand supramolecular enzyme mimic.

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 503-01-5