Cas 1279107-39-9,(4R,6S,7R)-7-ethyl 4-methyl 6-p-tolyl-5-azaspiro[2.4]heptane-4,7-dicarboxylate

1279107-39-9

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Basic information

Product Name: (4R,6S,7R)-7-ethyl 4-methyl 6-p-tolyl-5-azaspiro[2.4]heptane-4,7-dicarboxylate
Synonyms: (4R,6S,7R)-7-ethyl 4-methyl 6-p-tolyl-5-azaspiro[2.4]heptane-4,7-dicarboxylate
CAS NO:1279107-39-9
Molecular Formula:
Molecular Weight: 317.385
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: (4R,6S,7R)-7-ethyl 4-methyl 6-p-tolyl-5-azaspiro[2.4]heptane-4,7-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (4R,6S,7R)-7-ethyl 4-methyl 6-p-tolyl-5-azaspiro[2.4]heptane-4,7-dicarboxylate(1279107-39-9)
EPA Substance Registry System: (4R,6S,7R)-7-ethyl 4-methyl 6-p-tolyl-5-azaspiro[2.4]heptane-4,7-dicarboxylate(1279107-39-9)

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: 1279107-39-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1279107-39-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,9,1,0 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1279107-39:
(9*1)+(8*2)+(7*7)+(6*9)+(5*1)+(4*0)+(3*7)+(2*3)+(1*9)=169
169 % 10 = 9
So 1279107-39-9 is a valid CAS Registry Number.

1279107-39-9Upstream product

74592-36-2 ethyl cyclopropenylideneacetate

1279107-39-9Downstream Products

1279107-39-9Relevant academic research and scientific papers

Stereoselective construction of a 5-aza-spiro[2,4]heptane motif via catalytic asymmetric 1,3-dipolar cycloaddition of azomethine ylides and ethyl cyclopropylidene acetate

Liu, Tang-Lin,He, Zhao-Lin,Tao, Hai-Yan,Cai, Yue-Peng,Wang, Chun-Jiang

, p. 2616 - 2618 (2011)

A direct and facile synthesis of highly functional 5-aza-spiro[2,4] heptanes, a valuable structural motif for drug discovery, is developed via catalytic asymmetric 1,3-dipolar cycloaddition of cyclopropylidene acetate and azomethine ylides for the first t

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