Cas 135941-67-2,2-[(R)-3-Benzyloxycarbonylamino-4-(1H-indol-3-yl)-2-oxo-butyl]-malonic acid 2,5-dioxo-pyrrolidin-1-yl ester methyl ester

135941-67-2

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Basic information

Product Name: 2-[(R)-3-Benzyloxycarbonylamino-4-(1H-indol-3-yl)-2-oxo-butyl]-malonic acid 2,5-dioxo-pyrrolidin-1-yl ester methyl ester
Synonyms:
CAS NO:135941-67-2
Molecular Formula:
Molecular Weight: 549.537
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: 2-[(R)-3-Benzyloxycarbonylamino-4-(1H-indol-3-yl)-2-oxo-butyl]-malonic acid 2,5-dioxo-pyrrolidin-1-yl ester methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-[(R)-3-Benzyloxycarbonylamino-4-(1H-indol-3-yl)-2-oxo-butyl]-malonic acid 2,5-dioxo-pyrrolidin-1-yl ester methyl ester(135941-67-2)
EPA Substance Registry System: 2-[(R)-3-Benzyloxycarbonylamino-4-(1H-indol-3-yl)-2-oxo-butyl]-malonic acid 2,5-dioxo-pyrrolidin-1-yl ester methyl ester(135941-67-2)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 135941-67-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 135941-67-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,9,4 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 135941-67:
(8*1)+(7*3)+(6*5)+(5*9)+(4*4)+(3*1)+(2*6)+(1*7)=142
142 % 10 = 2
So 135941-67-2 is a valid CAS Registry Number.

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135941-67-2Relevant academic research and scientific papers

SYNTHESIS OF METHYL 6-ARALKYL-2,5-DIKETOPIPERIDINE-3-CARBOXYLATES AS SYNTHONS OF CONFORMATIONALLY CONSTRAINED PSEUDOPEPTIDES

Gomez-Monterrey, Isabel,Dominguez, M. Jose,Gonzalez-Muniz, Rosario,Harto, Juan R.,Garcia-Lopez, M. Teresa

, p. 3563 - 3564 (2007/10/02)

Catalytic hydrogenation of the 4-ketoesters 1a, b or 2a, b and their 5R-enantiomers, obtained from the corresponding Z-L- and Z-D-amino acid halomethyl ketones, directly leads to the methyl 6-aralkyl-2,5-diketopiperidine-3-carboxylates 3a, b and 4a, b and

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