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91571-48-1

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91571-48-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91571-48-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,5,7 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 91571-48:
(7*9)+(6*1)+(5*5)+(4*7)+(3*1)+(2*4)+(1*8)=141
141 % 10 = 1
So 91571-48-1 is a valid CAS Registry Number.

91571-48-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name aluminum oxyhydride

1.2 Other means of identification

Product number -
Other names -

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:91571-48-1 SDS

91571-48-1Downstream Products

91571-48-1Relevant articles and documents

Aluminumoxyhydride: Improved synthesis and application as a selective reducing agent

Tewari, Brij B.,Shekar, Sukesh,Huang, Longchuan,Gorrell, Carolyn E.,Murphy, Timothy P.,Warren, Kevin,Nesnas, Nasri,Wehmschulte, Rudolf J.

, p. 8807 - 8811 (2008/10/09)

Aluminumoxyhydride (HAlO) has been obtained by the reaction of aluminum hydride with the siloxane (Me2HSi)2O or the stannoxane (Bu3Sn)2O as an amorphous colorless insoluble powder. The highest-purity product resulted from the reaction of H3Al· NMe3 with (Me2HSi)2O. However, HAlO suspensions in tetrahydrofuran (THF) of sufficient quality for synthetic applications can be prepared from commercially available reagents with only minor precautions. A LiAlH4 solution in THF was treated successively with Me 3SiCl and (Me2HSi)2O, followed by heating at 60°C for 20 h. The resulting suspensions are 0.4-0.5 M in active hydride content and selectively reduce aldehydes and ketones to the respective alcohols in the presence of any other common nonprotic functional group.

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