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4-(1,2,2-Trimethylpropyl)morpholine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96921-32-3

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96921-32-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96921-32-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,9,2 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 96921-32:
(7*9)+(6*6)+(5*9)+(4*2)+(3*1)+(2*3)+(1*2)=163
163 % 10 = 3
So 96921-32-3 is a valid CAS Registry Number.

96921-32-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(3,3-dimethylbutan-2-yl)morpholine

1.2 Other means of identification

Product number -
Other names 4-(1,2,2-Trimethylpropyl)morpholine

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:96921-32-3 SDS

96921-32-3Downstream Products

96921-32-3Relevant academic research and scientific papers

Why Does the Intramolecular Trimethylene-Bridged Frustrated Lewis Pair Mes2PCH2CH2CH2B(C6F5)2 Not Activate Dihydrogen?

?zgün, Thomas,Ye, Ke-Yin,Daniliuc, Constantin G.,Wibbeling, Birgit,Liu, Lei,Grimme, Stefan,Kehr, Gerald,Erker, Gerhard

supporting information, p. 5988 - 5995 (2016/04/26)

The methyl labelled C3-bridged frustrated phosphane borane Lewis pair (P/B FLP) 2 b was prepared by treatment of Mes2PCl with a methallyl Grignard reagent followed by anti-Markovnikov hydroboration with Piers' borane [HB(C6/sub

Formic Acid Reduction of Enamines. Scope of the Reaction

Nilsson, Asa,Carlson, Rolf

, p. 187 - 190 (2007/10/02)

The scope of enamine reduction with formic acid has been investigated.The compounds studied include enamines from aldehydes, aliphatic ketones, aryl alkyl ketones and functionalized ketones.The procedure is simple and allows the reaction to be conducted without solvent.The method gives short reaction times and generally good yields of saturated amines.

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