Cas 688360-30-7,(S)-N-benzyloxycarbonyl-3-(4-hydroxy-3-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)phenyl)alanine methyl ester

688360-30-7

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Basic information

Product Name: (S)-N-benzyloxycarbonyl-3-(4-hydroxy-3-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)phenyl)alanine methyl ester
Synonyms: (S)-N-benzyloxycarbonyl-3-(4-hydroxy-3-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)phenyl)alanine methyl ester
CAS NO:688360-30-7
Molecular Formula:
Molecular Weight: 455.316
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: (S)-N-benzyloxycarbonyl-3-(4-hydroxy-3-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)phenyl)alanine methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-N-benzyloxycarbonyl-3-(4-hydroxy-3-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)phenyl)alanine methyl ester(688360-30-7)
EPA Substance Registry System: (S)-N-benzyloxycarbonyl-3-(4-hydroxy-3-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)phenyl)alanine methyl ester(688360-30-7)

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: 688360-30-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 688360-30-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,8,3,6 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 688360-30:
(8*6)+(7*8)+(6*8)+(5*3)+(4*6)+(3*0)+(2*3)+(1*0)=197
197 % 10 = 7
So 688360-30-7 is a valid CAS Registry Number.

688360-30-7Upstream product

688360-30-7Downstream Products

688360-31-8 (S)-N-benzyloxycarbonyl-3-(4-tert-butyldimethylsilyloxy-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)phenyl)alanine methyl ester

688360-30-7Relevant academic research and scientific papers

Preparation of selectively protected L-dopa derivatives: Oxidation of tyrosine-3-boronates

Hunter, Luke,Hutton, Craig A.

, p. 1095 - 1098 (2003)

Conversion of 3-iodo-L-tyrosine to protected tyrosine-3-boronate esters, followed by oxidation with hydrogen peroxide, provides a mild and efficient method for the preparation of selectively protected L-dopa derivatives.

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