Cas 214331-89-2,(2R,3R,4S)-2-Ethyl-3,4-dihydroxy-2-((S)-2-methoxymethyl-pyrrolidine-1-carbonyl)-4-methyl-cyclohexanone

214331-89-2

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Basic information

Product Name: (2R,3R,4S)-2-Ethyl-3,4-dihydroxy-2-((S)-2-methoxymethyl-pyrrolidine-1-carbonyl)-4-methyl-cyclohexanone
Synonyms: (2R,3R,4S)-2-Ethyl-3,4-dihydroxy-2-((S)-2-methoxymethyl-pyrrolidine-1-carbonyl)-4-methyl-cyclohexanone
CAS NO:214331-89-2
Molecular Formula:
Molecular Weight: 313.394
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (2R,3R,4S)-2-Ethyl-3,4-dihydroxy-2-((S)-2-methoxymethyl-pyrrolidine-1-carbonyl)-4-methyl-cyclohexanone(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R,4S)-2-Ethyl-3,4-dihydroxy-2-((S)-2-methoxymethyl-pyrrolidine-1-carbonyl)-4-methyl-cyclohexanone(214331-89-2)
EPA Substance Registry System: (2R,3R,4S)-2-Ethyl-3,4-dihydroxy-2-((S)-2-methoxymethyl-pyrrolidine-1-carbonyl)-4-methyl-cyclohexanone(214331-89-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 214331-89-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 214331-89-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,3,3 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 214331-89:
(8*2)+(7*1)+(6*4)+(5*3)+(4*3)+(3*1)+(2*8)+(1*9)=102
102 % 10 = 2
So 214331-89-2 is a valid CAS Registry Number.

214331-89-2Upstream product

210684-45-0 (2R,2'S)-2-ethyl-2-[[2'-(methoxymethyl)pyrrolidinyl]carbonyl]-4-methyl-cyclohex-3-en-1-one

214331-89-2Downstream Products

214331-89-2Relevant academic research and scientific papers

Stereoselective dihydroxylation of 2-alkyl- and 2,4-dialkyl-2-amido-3- cyclohexen-1-ones. Synthesis of enantiomerically related 2-alkyl- and 2,4- dialkyl-3-hydroxy-1-oxocyclohexan-2,4-carbolactones by complementary butyrolactonization reactions

Schultz, Arthur G.,Dai, Mingshi,Tham, Fook S.,Zhang, Xuqing

, p. 6663 - 6666 (2007/10/03)

Stereoselective dihydroxylation of 2a-2f gives cis-diols 3a-3f, from which hydroxylactones 5a-5f are obtained by an acid-catalyzed process involving retro aldol-realdolization prior to transesterification.

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