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113682-54-5

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113682-54-5 Usage

Physical form

White crystalline solid

Odor

Strong mint-like

Usage

Flavoring agent in food and beverages, fragrance additive in personal care products, production of perfumes

Toxicity

Possible carcinogen when consumed in large quantities or for prolonged periods of time

Health concerns

Companies are working to find alternative compounds to replace pulegone in their products.

Check Digit Verification of cas no

The CAS Registry Mumber 113682-54-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,6,8 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 113682-54:
(8*1)+(7*1)+(6*3)+(5*6)+(4*8)+(3*2)+(2*5)+(1*4)=115
115 % 10 = 5
So 113682-54-5 is a valid CAS Registry Number.

113682-54-5SDS

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 4,4,6,6-tetramethyl-5-azabicyclo[3.1.0]hexan-2-one

1.2 Other means of identification

Product number -
Other names 2,2,6,6-tetramethyl-1-azabicyclo[3.1.0]hexan-4-one

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:113682-54-5 SDS

113682-54-5Upstream product

113682-54-5Downstream Products

113682-54-5Relevant articles and documents

The effect of the nature of the substituent at the nitrogen atom on transformations of 3-bromo-2,2,6,6-tetramethyl-4-piperidinone and its 1-hydroxy and 1-oxyl derivatives under conditions of the Favorsky rearrangement

Krinitskaya

, p. 1140 - 1142 (1997)

3-Bromo-2,2,6,6-tetramethyl-4-oxopiperidine-1-oxyl reacts with NH4OH to give 3-carbamoyl-2,2,5,5-tetramethylpyrrolidine-1-oxyl, a product of the Favorsky rearrangement. 3-Bromo-2,2,6,6-tetramethyl-4-piperidinone is transformed under these conditions into a bicyclic amino ketone, while its 1-hydroxy derivative affords acyclic nitrosoenone.

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