Cas 6070-70-8,N-(2-hydroxyethyl)-2-[(4-oxo-3-phenyl-3,4,5,6,7,8-hexahydro[1]benzothieno[2,3-d]pyrimidin-2-yl)sulfanyl]acetamide

6070-70-8

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Basic information

Product Name: N-(2-hydroxyethyl)-2-[(4-oxo-3-phenyl-3,4,5,6,7,8-hexahydro[1]benzothieno[2,3-d]pyrimidin-2-yl)sulfanyl]acetamide
Synonyms: Acetamide, 2-[(3,4,5,6,7,8-hexahydro-4-oxo-3-phenyl[1]benzothieno[2,3-d]pyrimidin-2-yl)thio]-N-(2-hydroxyethyl)-; N-(2-Hydroxyethyl)-2-[(4-oxo-3-phenyl-3,4,5,6,7,8-hexahydro[1]benzothieno[2,3-d]pyrimidin-2-yl)sulfanyl]acetamide
CAS NO:6070-70-8
Molecular Formula: C₂₀H₂₁N₃O₃S₂
Molecular Weight: 415.529
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: 1.47g/cm³
Refractive Index: 1.733
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: N-(2-hydroxyethyl)-2-[(4-oxo-3-phenyl-3,4,5,6,7,8-hexahydro[1]benzothieno[2,3-d]pyrimidin-2-yl)sulfanyl]acetamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(2-hydroxyethyl)-2-[(4-oxo-3-phenyl-3,4,5,6,7,8-hexahydro[1]benzothieno[2,3-d]pyrimidin-2-yl)sulfanyl]acetamide(6070-70-8)
EPA Substance Registry System: N-(2-hydroxyethyl)-2-[(4-oxo-3-phenyl-3,4,5,6,7,8-hexahydro[1]benzothieno[2,3-d]pyrimidin-2-yl)sulfanyl]acetamide(6070-70-8)

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: 6070-70-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 6070-70-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,7 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6070-70:
(6*6)+(5*0)+(4*7)+(3*0)+(2*7)+(1*0)=78
78 % 10 = 8
So 6070-70-8 is a valid CAS Registry Number.

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6070-70-8Relevant academic research and scientific papers

A stereoselective synthesis of 3-substituted (S)-pyroglutamic and glutamic acids via OBO ester derivatives

Herdeis, Claus,Kelm, Bernd

, p. 217 - 229 (2007/10/03)

(S)-Pyroglutamic acid is transformed to the Cbz-protected 4-methyl-2,6,7-trioxabicyclo[2.2.2] octane (OBO) ester. This ortho ester functionality is employed as a bulky steering group for stereoselective introduction of alkyl and aryl groups via 1,4-cuprate addition to 3,4-unsaturated pyroglutamates. After deprotection and ringopening, 3-substituted glutamic acids are obtained.

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