Cas 1564245-75-5,(2S,3R)-methyl 2-((tert-butoxycarbonyl)amino)-3-(3-fluorophenyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propanoate

1564245-75-5

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Basic information

Product Name: (2S,3R)-methyl 2-((tert-butoxycarbonyl)amino)-3-(3-fluorophenyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propanoate
Synonyms: (2S,3R)-methyl 2-((tert-butoxycarbonyl)amino)-3-(3-fluorophenyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propanoate
CAS NO:1564245-75-5
Molecular Formula:
Molecular Weight: 423.29
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,3R)-methyl 2-((tert-butoxycarbonyl)amino)-3-(3-fluorophenyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propanoate(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3R)-methyl 2-((tert-butoxycarbonyl)amino)-3-(3-fluorophenyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propanoate(1564245-75-5)
EPA Substance Registry System: (2S,3R)-methyl 2-((tert-butoxycarbonyl)amino)-3-(3-fluorophenyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propanoate(1564245-75-5)

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: 1564245-75-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1564245-75-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,6,4,2,4 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1564245-75:
(9*1)+(8*5)+(7*6)+(6*4)+(5*2)+(4*4)+(3*5)+(2*7)+(1*5)=175
175 % 10 = 5
So 1564245-75-5 is a valid CAS Registry Number.

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1564245-75-5Relevant academic research and scientific papers

Copper-catalyzed asymmetric hydroboration of α-dehydroamino acid derivatives: Facile synthesis of chiral β-hydroxy-α-amino acids

He, Zhi-Tao,Zhao, Yi-Shuang,Tian, Ping,Wang, Chuan-Chuan,Dong, Han-Qing,Lin, Guo-Qiang

supporting information, p. 1426 - 1429 (2014/04/03)

The Cu-catalyzed asymmetric conjugate hydroboration reaction of β-substituted α-dehydroamino acid derivatives has been established, affording enantioenriched syn- and anti-β-boronate-α-amino acid derivatives with excellent combined yields (83-99%, dr ≈ 1:

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