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Furan, 3-[(4-methylphenyl)sulfinyl]-, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

143810-75-7

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143810-75-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 143810-75-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,8,1 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 143810-75:
(8*1)+(7*4)+(6*3)+(5*8)+(4*1)+(3*0)+(2*7)+(1*5)=117
117 % 10 = 7
So 143810-75-7 is a valid CAS Registry Number.

143810-75-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-(SS)-3-(p-tolylsulfinyl)furan

1.2 Other means of identification

Product number -
Other names (Ss)-3-(p-tolylsulfinyl)-furane

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:143810-75-7 SDS

143810-75-7Relevant academic research and scientific papers

Synthesis and photooxygenation of (S)-p-tolylsulfinylfuran derivatives

Arroyo, Yolanda,Carreno, M. Carmen,Garcia Ruano, Jose L.,Rodriguez Amo, Justo F.,Santos, Mercedes,Sanz Tejedor, M. Ascension

, p. 1183 - 1191 (2007/10/03)

The synthesis of different (S)-1,4-dicarbonyl-2-(p-tolylsulfinyl)-2-alkenes by photooxygenation of enantiomerically pure (S)-p-tolylsulfinylfurans is reported. Copyright (C) 2000.

Asymmetric synthesis of chiral sulfoxides and sulfinimines by using N-sulfinylsultam

Oppolzer, Wolfgang,Froelich, Olivier,Wiaux-Zamar, Chantal,Bernardinelli, Gerald

, p. 2825 - 2828 (2007/10/03)

Bornane-10,2-sultam 1 is stereoselectively converted by DMAP-assisted sulfinylation to diastereomerically pure (2R)-N-[(R)-p-tolylsulfinyl]-bornane-10,2-sultam 2 in 77% yield. The crystalline sulfinylating agent 2 reacts with a variety of nucleophiles to afford sulfoxides 3 and sulfinimines 5 in excellent yields and enantioselectivities.

Preparation of optically active 2-(or 3)(p-tolylsulfinyl)-3(or 2)furyl- or thienylcarboxaldehydes

Girodier,Maignan,Rouessac

, p. 2045 - 2052 (2007/10/03)

The preparation of the four enantiomerically pure title compounds is described by reaction of (I)-(-)-Ss-menthyl-p-toluenesulfinate on furan or thiophene precursors.

Syntheses of Enantiomerically Pure Furyl and Thienyl p-Tolyl Sulfoxides

Girodier, Laurent,Maignan, Christian,Rouessac, Francis

, p. 857 - 858 (2007/10/02)

We report a highly enantioselective reaction of Grignard reagents, derived from simple furans or thiophene, with (-)-(S)-menthylsulfinate to give in high yield enantiomerically pure furyl and thienylsulfoxides.

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