Cas 131226-66-9,(+)-(2S,4'R,6'R)-1-(10-tert-butyl-dimethylsilyloxy-1-trimethylsilyloxy-4,6-diphenyl-5-decylideneamino)-2-methoxymethyl-pyrrolidine

131226-66-9

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Basic information

Product Name: (+)-(2S,4'R,6'R)-1-(10-tert-butyl-dimethylsilyloxy-1-trimethylsilyloxy-4,6-diphenyl-5-decylideneamino)-2-methoxymethyl-pyrrolidine
Synonyms:
CAS NO:131226-66-9
Molecular Formula:
Molecular Weight: 639.082
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: (+)-(2S,4'R,6'R)-1-(10-tert-butyl-dimethylsilyloxy-1-trimethylsilyloxy-4,6-diphenyl-5-decylideneamino)-2-methoxymethyl-pyrrolidine(CAS DataBase Reference)
NIST Chemistry Reference: (+)-(2S,4'R,6'R)-1-(10-tert-butyl-dimethylsilyloxy-1-trimethylsilyloxy-4,6-diphenyl-5-decylideneamino)-2-methoxymethyl-pyrrolidine(131226-66-9)
EPA Substance Registry System: (+)-(2S,4'R,6'R)-1-(10-tert-butyl-dimethylsilyloxy-1-trimethylsilyloxy-4,6-diphenyl-5-decylideneamino)-2-methoxymethyl-pyrrolidine(131226-66-9)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 131226-66-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 131226-66-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,2,2 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 131226-66:
(8*1)+(7*3)+(6*1)+(5*2)+(4*2)+(3*6)+(2*6)+(1*6)=89
89 % 10 = 9
So 131226-66-9 is a valid CAS Registry Number.

131226-66-9Upstream product

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131226-66-9Relevant academic research and scientific papers

DIASTEREO- AND ENANTIOSELECTIVE SYNTHESIS OF α,α'-DISUBSTITUTED SPIROACETALS USING THE SAMP-/RAMP-HYDRAZONE METHOD

Enders, Dieter,Gatzweiler, Winfried,Dederichs, Eleonore

, p. 4757 - 4792 (2007/10/02)

α,α'-Disubstituted spiroacetals were synthesized with excellent enantiomeric excesses and in good overal yields from symmetrical ketones employing the SAMP-/RAMP-hydrazone-method for asymmetric α,α'-alkylation.

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