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15648-16-5

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15648-16-5 Usage

Uses

Reagent for: Labeling oligosaccharides for quantitative mass spectrometryAnalysis of sugar markers associated with Bacillus anthracis spores after cultureSynthesis of sulfated red seaweed galactan derived disaccharide alditolAnalysis of sulfated galactans from red algae by reductive hydrolysis and mild methanolysis by HPLCReactant for methanolic cleavageUsed in reductive pyrolysis of carrageenan by high performance anion-exchange chromatography

Check Digit Verification of cas no

The CAS Registry Mumber 15648-16-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,6,4 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15648-16:
(7*1)+(6*5)+(5*6)+(4*4)+(3*8)+(2*1)+(1*6)=115
115 % 10 = 5
So 15648-16-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H13BNO/c1-7(6)2-4-8-5-3-7/h2-6H2,1H3

15648-16-5 Well-known Company Product Price

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  • Aldrich

  • (262323)  Borane4-methylmorpholinecomplex  97%

  • 15648-16-5

  • 262323-5G

  • 768.69CNY

  • Detail

15648-16-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methylmorpholin-1-ium-1-yl)boron(1-)

1.2 Other means of identification

Product number -
Other names 4-methylmorpholine-borane (1/1)

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:15648-16-5 SDS

15648-16-5Relevant articles and documents

Crown-ether-catalysed synthesis of amine borane and amine trideuterioborane adducts from NaBH4-NaBD4 in ether

Kampel, V.,Warshawsky, A.

, p. 15 - 18 (2007/10/02)

Amine borane and amine trideuterioborane adducts have been obtained in good yield by the crown-ether-catalysed reaction of R3N*HCl with NaBH4 and NaBD4 in ether.The absence of isotopic exchange in the reaction with NaBD4 is demonstrated by IR and 11B and

Chemistry of boranes. XV. Synthesis of diborane from boric oxide

Ford,Kalb,Mcclelland,Muetterties

, p. 1032 - 1035 (2008/10/08)

A direct synthesis of diborane from boric oxide has been achieved by hydrogenation of the oxide in the presence of aluminum and aluminum trichloride. Very pure diborane is obtained from this reaction in 40-50% conversions at temperatures above 150° and hydrogen pressures of 750 atm. This hydrogenation is believed to proceed through an aluminum chlorohydride intermediate. Amine boranes, aminoboranes, and borazines were obtained directly from boric oxide when the hydrogenation was effected in the presence of secondary or tertiary alkylamines.

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