Cas 134866-01-6,[(4-amino-5,6-dimethylthieno[2,3-d]pyrimidin-2-yl)sulfanyl](phenyl)acetic acid

134866-01-6

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Basic information

Product Name: [(4-amino-5,6-dimethylthieno[2,3-d]pyrimidin-2-yl)sulfanyl](phenyl)acetic acid
Synonyms: [(4-amino-5,6-dimethylthieno[2,3-d]pyrimidin-2-yl)sulfanyl](phenyl)acetic acid
CAS NO:134866-01-6
Molecular Formula:
Molecular Weight: 345.446
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: [(4-amino-5,6-dimethylthieno[2,3-d]pyrimidin-2-yl)sulfanyl](phenyl)acetic acid(CAS DataBase Reference)
NIST Chemistry Reference: [(4-amino-5,6-dimethylthieno[2,3-d]pyrimidin-2-yl)sulfanyl](phenyl)acetic acid(134866-01-6)
EPA Substance Registry System: [(4-amino-5,6-dimethylthieno[2,3-d]pyrimidin-2-yl)sulfanyl](phenyl)acetic acid(134866-01-6)

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: 134866-01-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 134866-01-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,8,6 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 134866-01:
(8*1)+(7*3)+(6*4)+(5*8)+(4*6)+(3*6)+(2*0)+(1*1)=136
136 % 10 = 6
So 134866-01-6 is a valid CAS Registry Number.

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134866-01-6Relevant academic research and scientific papers

Analogs of a 4-aminothieno[2,3-d]pyrimidine lead (QB13) as modulators of P-glycoprotein substrate specificity

Haecker, Hans-Georg,Haye, Antje de la,Sterz, Katja,Schnakenburg, Gregor,Wiese, Michael,Guetschow, Michael

, p. 6102 - 6105 (2009)

P-glycoprotein (P-gp) is an important factor in the development of multidrug resistance (MDR) in cancer cells. In literature reports, a thieno[2,3-d]pyrimidine (QB13) was described as P-gp modulator and opposed effects on the cell accumulation of distinct

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