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Ethanone, 1-(tetrahydro-5-hydroxy-4-methyl-3-furanyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

113531-95-6

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113531-95-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113531-95-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,5,3 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 113531-95:
(8*1)+(7*1)+(6*3)+(5*5)+(4*3)+(3*1)+(2*9)+(1*5)=96
96 % 10 = 6
So 113531-95-6 is a valid CAS Registry Number.

113531-95-6SDS

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 (+/-)-botryodiplodin

1.2 Other means of identification

Product number -
Other names (2RS,3SR)-3-hydroxymethyl-2-methyl-4-oxo-pentanal (

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:113531-95-6 SDS

113531-95-6Relevant academic research and scientific papers

Synthesis of (±)- and (-)-botryodiplodin using stereoselective radical cyclizations of acyclic esters and acetals

Nouguier, Robert,Gastaldi, Stephane,Stien, Didier,Bertrand, Michele,Villar, Felix,Andrey, Olivier,Renaud, Philippe

, p. 3005 - 3018 (2007/10/03)

Three different routes for the stereoselective synthesis of botryodiplodin have been investigated. The intramolecular allylation of acetals proved to be unsatisfactory due to unstable intermediates and poor stereocontrol. Zard intramolecular radical allyl

Intramolecular radical allylation with allylic sulfones a synthesis of (±)-botryodiplodin

Nouguier, Robert,Gastaldi, Stephane,Stien, Didier,Bertrand, Michele,Renaud, Philippe

, p. 3371 - 3374 (2007/10/03)

Isopropenyl-5-membered-ring acetal or lactone are potential precursors of (±)-botryodiplodin (1). Several pathways, involving 5-exo-trig ring closure onto allylic sulfones, have been investigated. The iodine atom transfer methodology allowed the preparati

Diastereoselective radical cyclization of bromoacetals: Efficient synthesis of (±)-botryodiplodin

Villar, Felix,Andrey, Olivier,Renaud, Philippe

, p. 3375 - 3378 (2007/10/03)

A stereoselective synthesis of (±)-botryodiplodin is presented. The key reaction is a radical cyclization of a bromoacetal (Ueno-Stork reaction). The stereogenic acetal center has been used to control the stereoselectivity of the process: the difficulty in controlling the stereochemistry at C(3) of the tetrahydrofuran moiety during the cyclization step has been overcome by a double one-pot reduction procedure starting from a gem-dibromide.

Acyclic Stereoselection in the Ortho Ester Claisen Rearrangement

Daub, G. William,Edwards, James P.,Okada, Carol R.,Allen, Jana Westran,Maxey, Claudia Tata,Wells, Matthew S.,Goldstein, Alexandra S.,Dibley, Michael J.,Wang, Clarence J.,Ostercamp, Daniel P.,Chung, Steven,Cunningham, Paula Shanklin,Berliner, Martin A.

, p. 1976 - 1985 (2007/10/03)

The ortho ester Claisen rearrangement of trisubstituted allylic alcohols exhibits significant levels of diastereoselection. In E allylic alcohols, a 1,3-diaxial interaction develops in the chairlike transition state leading to the anti isomer, rendering the reaction syn selective by a factor of 3-5 to 1. In Z allylic alcohols, the 1,3-diaxial interaction develops in the transition state leading to the syn isomer, generating an anti:syn selectivity of 6-15 to 1. The relative stereochemistry of the syn isomer was confirmed independently by the synthesis of the mycotoxin botryodiplodin.

Total Synthesis of (-)- and (+)-Botryodiplodin and (+)- and (-)-Epibotryodiplodin

Rehnberg, Nicola,Magnusson, Goeran

, p. 377 - 383 (2007/10/02)

the title compounds were prepared by the conjugate addition (d.e. more than 94percent) of LiMeCNCu to the chiral isoprene units (+)-(2R)- and (-)-(2S)-benzyloxy-2,5-dihydrofuran-4-carboxaldehyde (1r and 1s) followed by methyllithium-attack on the mixture

DIASTEREOSELECTIVE CONJUGATE ADDITION OF LITHIUM METHYLCYANOCUPRATE TO THE CHIRAL ISOPRENE UNITS 2-(R)- AND (S)-BENZYLOXY-2,5-DIHYDRO-4-FURANCARBOXALDEHYDE. TOTAL SYNTHESIS OF (-)- AND (+)-BOTRYODIPLODIN AND (+)- AND (-)-EPIBOTRYODIPLODIN.

Rehnberg, Nicola,Frejd, Torbjoern,Magnusson, Goeran

, p. 3589 - 3592 (2007/10/02)

Conjugate addition of lithium methylcyanocuprate to the title aldehydes proceeded with high diastereoselectivity (d.e. 94percent).Methyl lithium 1,2-addition, followed by Swern oxidation of the resulting alcohols, gave benzyl botryodiplodin and benzyl epi

Acyclic Stereocontrol through the Dianionic Claisen Rearrangement of β-Hydroxy Esters: Synthesis of (+/-)-Botryodiplodin

Kurth, Mark J.,Yu, Chan-Mo

, p. 1840 - 1845 (2007/10/02)

Dianionic Claisen rearrangements of (E)- and (Z)-butenyl β-hydroxy esters afford moderate stereoselection in the construction of highly functionalized acyclic systems.The reaction proceeds with remote stereocontrol and the resulting products display three contiguous chiral centers, C(α) and C(β') stereocenters being established in the rearrangement (cf. 1z -> 3b).Experiments are described which unambiguously establish that each dianionic Claisen proceeds with excellent diastereoface selectivity and moderate chair/boat selectivity .Application of this Claisen protocol to a synthesis of the mycotoxin botryodiplodin is also described (1z -> 8b).

BIOSYNTHESE DE LA BOTRYODIPLODINE, MYCOTOXINE DE PENICILLIUM ROQUEFORTI: INCORPORATIONS D'ACETATE13C>, 13C>, 13C> ET D'ACIDE ORSELLINIQUE13C-CARBOXYLE13>, 13C>

Renauld, F.,Moreau, S.

, p. 1823 - 1834 (2007/10/02)

Incorporations of 13C>, 13C>, 13C> acetate and 13C, carboxyl-13C>, 13C> orsellinic acid into botryodiplodin indicate that this mycotoxin is biosynthesized by the polyketide pathway.Orsellinic acid is a precursor of botryodiplodin.A biosynthetic pathway, using orsellinic acid as precursor, is proposed.

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