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Cyclopenta[c]pyran-1(3H)-one,4,4a,5,6-tetrahydro- 4,7-dimethyl-,(4R,4aR)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76549-18-3

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76549-18-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76549-18-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,4 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 76549-18:
(7*7)+(6*6)+(5*5)+(4*4)+(3*9)+(2*1)+(1*8)=163
163 % 10 = 3
So 76549-18-3 is a valid CAS Registry Number.

76549-18-3Downstream Products

76549-18-3Relevant academic research and scientific papers

Extracyclic Stereocontrol in Addition Reaction of Crotylsilanes with 2-Substituted 2-Cyclopentenones. Stereodivergent Synthesis of (+)-Neonepetalacton and (+)-Isoneonepetalactone

Pan, Li-Rui,Tokoroyama, Takashi

, p. 1999 - 2002 (1990)

The addition reaction of E- and Z-crotylsilanes with 2-substituted 2-cyclopentenones showed the preference of erythro and threo products respectively.The refinement of the selectivity was investigated and the result was utilized for efficient syntheses of

Reaction of Organoaluminium Reagents with Cyclopropylmethyl Acetates and 2-Vinylcyclopropane-1,1-dicarboxylate Esters

Hiyama, Tamejiro,Morizawa, Yoshitomi,Yamamoto, Hajime,Nozaki, Hitosi

, p. 2151 - 2160 (2007/10/02)

Ring-opening alkylation of cyclopropylmethyl acetates was studied.The acetoxyl group of 7-(1-acetoxyheptyl)norcarane is substituted by the alkyl group upon treatment with trialkylaluminium, but alkylation of trans-1-(1-acetoxyethyl)-2-phenylcyclopropane with trialkylaluminium gives rise to trans-5-phenyl-2-alkenes.The reaction of (1S,2S)-2-phenylcyclopropylmethyl acetate with trimethylaluminium resulted in the complete loss of optical activity to give racemic 4-phenyl-1-pentene.Alkylation of trans-1-(1-acetoxy-3-phenylpropyl)-2-vinylcyclopropane with trialkylaluminium proceeds under regioselective ring-opening to give 3-alkylated trans-8-phenyl-1,5-octadiene (selectivity 73-83percent).The regio- and stereochemistry of homoconjugate addition to activated vinylcyclopropanes having a doubly carbonyl substituted ring carbon was studied.Trialkylaluminium on addition to diethyl 2-vinylcyclopropane-1,1-dicarboxylate in a 1,5-manner afford diethyl (2-alkyl-3-butenyl)propanedioate (over 96percent selectivity).In contrast, the reaction of this cyclopropane with tetraalkylaluminiumlithium takes place in a 1.7-manner to give diethyl (trans-4-alkyl-2-butenyl)propanedioate with 88-92percent selectivity.Clean regiocontrol of the reaction is observed in the methylation of ethyl exo-6-(trans-1-propenyl)-2-oxobicyclo(3.1.0>hexane-1-carboxylate with trimethylaluminium or tetramethyl aluminiumlithium.Alkylation with trimethylaluminium proceeds with 86percent inversion of the configuration at C(6) of the substrate, affording (2R*,3R*)-2-ethoxycarbonyl-3-cyclopentanone which is transformed into neonepetalactone.

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