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30885-14-4

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30885-14-4 Usage

Type of compound

Bicyclic guanidine derivative

Usage

Catalyst in organic synthesis

Structural feature

Bulky and sterically hindered due to the presence of tert-butyl groups

Efficiency

Highly efficient catalyst for a variety of reactions

Reactions promoted

Nucleophilic substitution, Michael addition, and cycloaddition

Specialized application

Catalyzing the formation of carbon-carbon bonds

Molecular structure

Unique

Catalytic properties

Versatile

Value

Valuable tool in the field of organic chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 30885-14-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,8,8 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 30885-14:
(7*3)+(6*0)+(5*8)+(4*8)+(3*5)+(2*1)+(1*4)=114
114 % 10 = 4
So 30885-14-4 is a valid CAS Registry Number.

30885-14-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-ditert-butyl-1,3-diazetidine-2,4-dione

1.2 Other means of identification

Product number -
Other names N,N'-di-tert-butyldiazetidinedione

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:30885-14-4 SDS

30885-14-4Downstream Products

30885-14-4Relevant articles and documents

Novel synthesis of diazetidine-2,4-dione by ring expansion of diaziridinone

Komatsu, Mitsuo,Tamabuchi, Satoshi,Minakata, Satoshi,Ohshiro, Yoshiki

, p. 67 - 70 (2007/10/03)

Treatment of N,N'-di-tert-butyldiaziridinone with Ni(CO)4 under an atmosphere of carbon monoxide caused a carbonylative ring expansion to give ditert-butyldiazetidinedione in good yield. In the presence of diphenylketene under the conditions, azetidinedione derivative was obtained.

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