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1113-78-6

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1113-78-6 Usage

Chemical Properties

Colorless liquid

Check Digit Verification of cas no

The CAS Registry Mumber 1113-78-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,1 and 3 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1113-78:
(6*1)+(5*1)+(4*1)+(3*3)+(2*7)+(1*8)=46
46 % 10 = 6
So 1113-78-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H27B/c1-7-10(4)13(11(5)8-2)12(6)9-3/h10-12H,7-9H2,1-6H3

1113-78-6 Well-known Company Product Price

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  • Aldrich

  • (178969)  Tri-sec-butylboranesolution  1.0 M in THF

  • 1113-78-6

  • 178969-100ML

  • 1,539.72CNY

  • Detail

1113-78-6SDS

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 Tris(1-methylpropyl)borane

1.2 Other means of identification

Product number -
Other names tri(butan-2-yl)borane

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:1113-78-6 SDS

1113-78-6Relevant articles and documents

Hennion et al.

, p. 5190 (1957)

Pd-catalyzed three-component reaction of 3-(Pinacolatoboryl)ally acetates, aldehydes, and organoboranes: A new entry to stereoselective synthesis of (Z)- anti -homoallylic alcohols

Horino, Yoshikazu,Aimono, Ataru,Abe, Hitoshi

supporting information, p. 2824 - 2827 (2015/06/16)

The Pd-catalyzed three-component reaction of 3-(pinacolatoboryl)allyl acetates, aldehydes, and organoboranes is described. The reaction is initiated by the formation of an allylic gem-palladium/boryl intermediate, which then undergoes allylation of aldehydes by allylboronates followed by a coupling reaction of in situ generated (Z)-vinylpalladium acetates with organoboranes to provide the (Z)-anti-homoallylic alcohols with high levels of diastereoselectivity and alkene stereocontrol.

Protic acid behavior of phosphine-triborane(7)

DePoy, Rosemarie E.,Kodama, Goji

, p. 4077 - 4079 (2008/10/08)

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