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6496-56-6

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6496-56-6 Usage

Type of compound

Highly stable and non-reactive cyclic amine

Common use

Strong, non-nucleophilic base in organic synthesis

Additional use

Solvent for a wide range of organic compounds

Physical state

Colorless liquid

Odor

Mild amine odor

Toxicity

Relatively non-toxic

Industrial applications

Suitable for various industrial applications

Stability

Stable under a wide range of conditions

Fields of application

Pharmaceuticals, agrochemicals, and specialty chemicals

Advantages

Precise control over reaction conditions and product purity

Check Digit Verification of cas no

The CAS Registry Mumber 6496-56-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,9 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6496-56:
(6*6)+(5*4)+(4*9)+(3*6)+(2*5)+(1*6)=126
126 % 10 = 6
So 6496-56-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H19N/c1-8(2)6-7-9(3,4)10(8)5/h6-7H2,1-5H3

6496-56-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,2,5,5-pentamethylpyrrolidine

1.2 Other means of identification

Product number -
Other names Pyrrolidine,1,2,2,5,5-pentamethyl

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:6496-56-6 SDS

6496-56-6Downstream Products

6496-56-6Relevant articles and documents

RING-OPENING REACTIONS. VII. RING-SIZE EFFECTS ON THE REACTIVITIES OF 1,1,2,2,ω,ω-HEXAMETHYL CYCLIC AMMONIUM IONS IN THE EXOCYCLIC ELIMINATION REACTION

Frachey, Giuseppe,Gionta, Grazia,Lillocci, Claudio

, p. 463 - 466 (2007/10/02)

The reactivities of cyclic ammonium ions (3-,4-,5-, and 6-membered rings) have been determined in a ring-opening elimination reaction.The comparison with analogous reactivity data obtained in previous work on the ring opening substitution reaction suggests a substantial difference in the effect of the stereochemical factors governing the two ring-opening reactions and confirms the anomalous behaviour of small rings in the ring-opening substitution reaction.

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