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126741-70-6

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126741-70-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126741-70-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,7,4 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 126741-70:
(8*1)+(7*2)+(6*6)+(5*7)+(4*4)+(3*1)+(2*7)+(1*0)=126
126 % 10 = 6
So 126741-70-6 is a valid CAS Registry Number.

126741-70-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[tert-butyl(diphenyl)silyl]prop-2-yn-1-ol

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:126741-70-6 SDS

126741-70-6Relevant articles and documents

Gold(i)-catalyzed pathway-switchable tandem cycloisomerizations to indolizino[8,7-: B] indole and indolo[2,3-a] quinolizine derivatives

Liu, Chengjun,Sun, Zenghui,Xie, Fukai,Liang, Guoduan,Yang, Lu,Li, Yaqiao,Cheng, Maosheng,Lin, Bin,Liu, Yongxiang

supporting information, p. 14418 - 14421 (2019/12/05)

Experimental and theoretical explorations were performed on the pathways of the cascade cycloisomerizations of tryptamine-N-ethynylpropiolamide substrates. The methodology provided a common strategy to access either indolizino[8,7-b]indoles or indolo[2,3-

Reactivity pattern of bis(propargyloxy) disulfides: Tandem rearrangements and cyclizations

Braverman, Samuel,Pechenick-Azizi, Tatiana,Gottlieb, Hugo E.,Sprecher, Milon

, p. 1741 - 1750 (2011/07/09)

Thirty-five substituted bis(propargyloxy) disulfides were successfully prepared in good to excellent yields, and their reactivity was found to be strongly dependent on the substitution pattern of the reactant. Inter alia they undergo surprising tandem sigmatropic rearrangements and cycloadditions. Three heretofore unknown product types were isolated and fully characterized: 6,7-dithiabicyclo[3.1.1]heptan-2-one 6-oxide derivatives, two isomeric 1,2-dithiete 1,1-dioxides (α,β-unsaturated four-membered cyclic thiosulfonates) from bis(propargyloxy) disulfides with α- or γ-alkyl-substituted propargyl groups, and two isomeric 2-oxa-5,7-dithiabicyclo[2.2.1]heptane 5-oxides from bis(propargyloxy) disulfides with α-tert-butyl- or α,α-dialkyl-substituted propargyl groups. Georg Thieme Verlag Stuttgart - New York.

Reaction of δ-silyl-γ,δ-epoxy-α,β-unsaturated acylsilanes with cyanide ion: Possibility of the formation of silicate intermediate in anion-induced ring opening of epoxysilanes

Tanaka, Koudai,Masu, Hyuma,Yamaguchi, Kentaro,Takeda, Kei

, p. 6429 - 6432 (2007/10/03)

Reaction of trans- and cis-δ-silyl-γ,δ-epoxy-α, β-unsaturated acylsilanes 1 and 9 with cyanide ion in the presence of an electrophile affords double Brook rearrangement products 10 in an E/Z ratio depending on the cis/trans geometry of the epoxysilanes.

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