Cas 197907-47-4,Bromo-acetic acid (1S,4R)-4-(4-methoxy-phenoxy)-1-methyl-5-oxo-pentyl ester

197907-47-4

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Basic information

Product Name: Bromo-acetic acid (1S,4R)-4-(4-methoxy-phenoxy)-1-methyl-5-oxo-pentyl ester
Synonyms: Bromo-acetic acid (1S,4R)-4-(4-methoxy-phenoxy)-1-methyl-5-oxo-pentyl ester
CAS NO:197907-47-4
Molecular Formula:
Molecular Weight: 359.217
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: Bromo-acetic acid (1S,4R)-4-(4-methoxy-phenoxy)-1-methyl-5-oxo-pentyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Bromo-acetic acid (1S,4R)-4-(4-methoxy-phenoxy)-1-methyl-5-oxo-pentyl ester(197907-47-4)
EPA Substance Registry System: Bromo-acetic acid (1S,4R)-4-(4-methoxy-phenoxy)-1-methyl-5-oxo-pentyl ester(197907-47-4)

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: 197907-47-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 197907-47-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,7,9,0 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 197907-47:
(8*1)+(7*9)+(6*7)+(5*9)+(4*0)+(3*7)+(2*4)+(1*7)=194
194 % 10 = 4
So 197907-47-4 is a valid CAS Registry Number.

197907-47-4Upstream product

192992-65-7 Bromo-acetic acid (1S,4R)-5,5-diethoxy-4-(4-methoxy-phenoxy)-1-methyl-pentyl ester

197907-47-4Downstream Products

197907-47-4Relevant academic research and scientific papers

A total synthesis of the (5R,8S,13R,16S)-isomer of gyrenophorol

Amigoni,Le Floc'h

, p. 2827 - 2831 (1997)

The first total synthesis of the (5R,8S,13R,16S)-isomer 3 of pyrenophorol is described using a retrosynthetic scheme based on two consecutive double bond cleavages. The title compound 3 was prepared in 14 steps with an overall yield of 4.5% starting from

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