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diethylaluminium diisopropylamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68006-53-1

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68006-53-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68006-53-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,0,0 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 68006-53:
(7*6)+(6*8)+(5*0)+(4*0)+(3*6)+(2*5)+(1*3)=121
121 % 10 = 1
So 68006-53-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H14N.2C2H5.Al/c1-5(2)7-6(3)4;2*1-2;/h5-6H,1-4H3;2*1H2,2H3;/q3*-1;+3

68006-53-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name diethylalumanylium,di(propan-2-yl)azanide

1.2 Other means of identification

Product number -
Other names diethylalumanylium

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:68006-53-1 SDS

68006-53-1Upstream product

68006-53-1Downstream Products

68006-53-1Relevant academic research and scientific papers

Azetidinone compounds useful in the preparation of carbapenem antibiotics and process for preparing carbapenem and penem compounds

-

, (2008/06/13)

Compounds of formula (I): STR1 wherein: R1 is hydrogen or a hydroxy-protecting group; R2 is alkyl, alkoxy, halogen, optionally substituted phenyl or optionally substituted phenoxy; R3 is optionally substituted pyridyl, optionally substituted quinolyl or phenyl group which has a substituent of formula --CYNR5 R6, where Y is oxygen or sulfur, and R5 and R6 are each alkyl, aryl or aralkyl, or R5 and R6 and the nitrogen to which they are attached together form a heterocyclic group; is R4 hydrogen or an amino-protecting group; and Z is sulfur or oxygen; are valuable intermediates in the preparation of carbapenem compounds and retain a desirable configuration during conversion to such carbapenem compounds. Penem and carbapenem compounds having a group of formula --SA' are prepared from a corresponding compound having a substituted thio, sulfinyl or sulfonyl group at this position by reaction with a compound A'SH (where A' is an organic group) in the presence of a salt of a metal of Group II or III of the Periodic Table.

Process for preparing carbapenem and penem compounds and new compounds involved in that process

-

, (2008/06/13)

Penem and carbapenem compounds having a group of formula -SA are prepared from a corresponding compound having a substituted thio, sulphinyl or sulphonyl group at this position by reaction with a compound ASH (where A is various organic groups) in the presence of a salt of a metal of Group II or III of the Periodic Table.

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