Cas 607358-40-7,2-<i>tert</i>-butoxycarbonylamino-3-hydroxy-3-(4-hydroxy-phenyl)-thiopropionic acid <i>S</i>-(2-acetylamino-ethyl) ester

607358-40-7

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Basic information

Product Name: 2-tert-butoxycarbonylamino-3-hydroxy-3-(4-hydroxy-phenyl)-thiopropionic acid S-(2-acetylamino-ethyl) ester
Synonyms: 2-tert-butoxycarbonylamino-3-hydroxy-3-(4-hydroxy-phenyl)-thiopropionic acid S-(2-acetylamino-ethyl) ester
CAS NO:607358-40-7
Molecular Formula:
Molecular Weight: 398.48
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-tert-butoxycarbonylamino-3-hydroxy-3-(4-hydroxy-phenyl)-thiopropionic acid S-(2-acetylamino-ethyl) ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-tert-butoxycarbonylamino-3-hydroxy-3-(4-hydroxy-phenyl)-thiopropionic acid S-(2-acetylamino-ethyl) ester(607358-40-7)
EPA Substance Registry System: 2-tert-butoxycarbonylamino-3-hydroxy-3-(4-hydroxy-phenyl)-thiopropionic acid S-(2-acetylamino-ethyl) ester(607358-40-7)

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: 607358-40-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 607358-40-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,7,3,5 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 607358-40:
(8*6)+(7*0)+(6*7)+(5*3)+(4*5)+(3*8)+(2*4)+(1*0)=157
157 % 10 = 7
So 607358-40-7 is a valid CAS Registry Number.

607358-40-7Upstream product

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607358-40-7Relevant academic research and scientific papers

Synthesis of proposed oxidation-cyclization-methylation intermediates of the coumarin antibiotic biosynthetic pathway

Tao, Junhua,Hu, Shanghui,Pacholec, Michelle,Walsh, Christopher T.

, p. 3233 - 3236 (2007/10/03)

(Matrix presented) A chemoenzymatic synthesis was described to prepare proposed oxidation-cyclization-methylation intermediates of the coumarin antibiotic biosynthetic pathway. The successful synthesis of these fragile molecules relies heavily on mild enz

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