Cas 263752-01-8,N-[(1S,2S)-3-Benzyloxy-1-benzyloxymethyl-2-(2,2-dimethyl-propionylamino)-propyl]-2,2-dimethyl-propionamide

263752-01-8

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Basic information

Product Name: N-[(1S,2S)-3-Benzyloxy-1-benzyloxymethyl-2-(2,2-dimethyl-propionylamino)-propyl]-2,2-dimethyl-propionamide
Synonyms: N-[(1S,2S)-3-Benzyloxy-1-benzyloxymethyl-2-(2,2-dimethyl-propionylamino)-propyl]-2,2-dimethyl-propionamide
CAS NO:263752-01-8
Molecular Formula:
Molecular Weight: 468.637
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: N-[(1S,2S)-3-Benzyloxy-1-benzyloxymethyl-2-(2,2-dimethyl-propionylamino)-propyl]-2,2-dimethyl-propionamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[(1S,2S)-3-Benzyloxy-1-benzyloxymethyl-2-(2,2-dimethyl-propionylamino)-propyl]-2,2-dimethyl-propionamide(263752-01-8)
EPA Substance Registry System: N-[(1S,2S)-3-Benzyloxy-1-benzyloxymethyl-2-(2,2-dimethyl-propionylamino)-propyl]-2,2-dimethyl-propionamide(263752-01-8)

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: 263752-01-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 263752-01-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,3,7,5 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 263752-01:
(8*2)+(7*6)+(6*3)+(5*7)+(4*5)+(3*2)+(2*0)+(1*1)=138
138 % 10 = 8
So 263752-01-8 is a valid CAS Registry Number.

263752-01-8Upstream product

263752-01-8Downstream Products

263752-01-8Relevant academic research and scientific papers

Asymmetric cyclopropanation catalyzed by C2-symmetric bi(oxazolines)

Boulch, Rachel,Scheurer, Andreas,Mosset, Paul,Saalfrank, Rolf W.

, p. 1023 - 1026 (2007/10/03)

C2-symmetric bi(oxazolines) 3a-e were prepared in three steps based on a tartaric-derived vicinal diamine as common precursor. These chiral ligands were studied with respect to their directive influence on the enantioselective copper catalyzed

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