Cas 354798-38-2,3-[bis-(3,5-dimethyl-phenyl)-phosphanyl]-2-<i>tert</i>-butoxycarbonylamino-propionic acid methyl ester

354798-38-2

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Basic information

Product Name: 3-[bis-(3,5-dimethyl-phenyl)-phosphanyl]-2-tert-butoxycarbonylamino-propionic acid methyl ester
Synonyms: 3-[bis-(3,5-dimethyl-phenyl)-phosphanyl]-2-tert-butoxycarbonylamino-propionic acid methyl ester
CAS NO:354798-38-2
Molecular Formula:
Molecular Weight: 443.523
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: 3-[bis-(3,5-dimethyl-phenyl)-phosphanyl]-2-tert-butoxycarbonylamino-propionic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3-[bis-(3,5-dimethyl-phenyl)-phosphanyl]-2-tert-butoxycarbonylamino-propionic acid methyl ester(354798-38-2)
EPA Substance Registry System: 3-[bis-(3,5-dimethyl-phenyl)-phosphanyl]-2-tert-butoxycarbonylamino-propionic acid methyl ester(354798-38-2)

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: 354798-38-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 354798-38-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,4,7,9 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 354798-38:
(8*3)+(7*5)+(6*4)+(5*7)+(4*9)+(3*8)+(2*3)+(1*8)=192
192 % 10 = 2
So 354798-38-2 is a valid CAS Registry Number.

354798-38-2Upstream product

354798-38-2Downstream Products

354798-38-2Relevant academic research and scientific papers

High asymmetric induction with β-turn-derived palladium phosphine complexes

Greenfield, Scott J.,Agarkov, Anton,Gilbertson, Scoff R.

, p. 3069 - 3072 (2003)

(Matrix presented) Work toward the development of a bisphosphine ligand system for the palladium-catalyzed addition to cyclic allyl acetates is reported. A parallel approach using phosphine-containing amino acids in conjunction with natural amino acids wa

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