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2-Butanone, 3-[(2R,4R,5S)-2-(4-methoxyphenyl)-5-methyl-1,3-dioxan-4-yl]-, (3R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

652986-45-3

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652986-45-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 652986-45-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,2,9,8 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 652986-45:
(8*6)+(7*5)+(6*2)+(5*9)+(4*8)+(3*6)+(2*4)+(1*5)=203
203 % 10 = 3
So 652986-45-3 is a valid CAS Registry Number.

652986-45-3SDS

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 (3R,4R,5S)-4,6-[(R)-4-methoxy-benzylidenedioxy]-3,5-dimethyl-2-butanone

1.2 Other means of identification

Product number -
Other names (R)-3-[(2R,4R,5S)-2-(4-Methoxy-phenyl)-5-methyl-[1,3]dioxan-4-yl]-butan-2-one

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:652986-45-3 SDS

652986-45-3Downstream Products

652986-45-3Relevant academic research and scientific papers

Synthesis of C3-C21 Segment of Aflastatin A Using Remote Asymmetric Induction Reactions

Murakoshi, Sawato,Hosokawa, Seijiro

supporting information, p. 758 - 761 (2019/01/21)

The C3-C21 segment of aflastatin A has been synthesized by converging three segments including the C3-C8 segment, the C9-C15 segment, and the C16-C21 segment. Each segment has been synthesized from a vinylketene silyl N,O-acetal possessing a chiral auxili

Crotylsilane reagents in the synthesis of complex polyketide natural products: Total synthesis of (+)-discodermolide

Arefolov, Alexander,Panek, James S.

, p. 5596 - 5603 (2007/10/03)

An efficient, highly convergent stereocontrolled synthesis of (+)-discodermolide has been achieved with 2.1% overall yield (27 steps longest linear sequence). The absolute stereochemistry of the C1-C6 (12), C7-C14 (13), and C15-C24 (11) subunits was intro

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