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91266-03-4

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91266-03-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91266-03-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,2,6 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 91266-03:
(7*9)+(6*1)+(5*2)+(4*6)+(3*6)+(2*0)+(1*3)=124
124 % 10 = 4
So 91266-03-4 is a valid CAS Registry Number.

91266-03-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl-pent-4-ynoxy-diphenylsilane

1.2 Other means of identification

Product number -
Other names Silane,(1,1-dimethylethyl)(4-pentynyloxy)diphenyl

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:91266-03-4 SDS

91266-03-4Relevant articles and documents

Survey of synthetic approaches to natural (peyssonenynes) and unnatural acetoxyenediynes

Garcia-Dominguez, Patricia,Alvarez, Rosana,De Lera, Angel R.

, p. 4762 - 4782 (2012)

Four convergent synthetic approaches to acetoxyenediynes have been explored to gain access to peyssonenynes A and B, which are natural products isolated from the red alga Peyssonelia caulifera. After optimization of the routes with a palmitic acid based m

Enantioselective Catalytic Crotylboration Based Syntheses of the C(7)–C(18(20)) Fragments of Polyketides Isolated from Streptomyces gramineus

Morávková, Terézia,Bedná?ová, Eva,Kotora, Martin

, (2021/10/20)

A general modular enantioselective synthetic approach to the C(7)–C(18) and the C(7)–C(20) fragment belonging to E-492, actinofuranone A, and JBIR-108 was developed. The crucial synthetic step relies on highly enantioselective crotylboration of aldehydes

A bio-inspired cascade and a late-stage directed sp3 C–H lithiation enables a concise total synthesis of (?)-virosaine A

Hughes, Jonathan M.E.,Gleason, James L.

supporting information, p. 759 - 768 (2018/01/01)

The asymmetric total synthesis of (?)-virosaine A was achieved in 9% overall yield from commercially/readily available starting materials. Inspired by an intriguing biosynthetic proposal, a novel cascade reaction sequence was developed to efficiently cons

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