Cas 1025902-00-4,(R)-3-Hydroxymethyl-6,7,8-trimethoxy-2-((R)-2-methoxy-1-phenyl-ethyl)-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid

1025902-00-4

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Basic information

Product Name: (R)-3-Hydroxymethyl-6,7,8-trimethoxy-2-((R)-2-methoxy-1-phenyl-ethyl)-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid
Synonyms:
CAS NO:1025902-00-4
Molecular Formula:
Molecular Weight: 431.486
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: (R)-3-Hydroxymethyl-6,7,8-trimethoxy-2-((R)-2-methoxy-1-phenyl-ethyl)-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid(CAS DataBase Reference)
NIST Chemistry Reference: (R)-3-Hydroxymethyl-6,7,8-trimethoxy-2-((R)-2-methoxy-1-phenyl-ethyl)-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid(1025902-00-4)
EPA Substance Registry System: (R)-3-Hydroxymethyl-6,7,8-trimethoxy-2-((R)-2-methoxy-1-phenyl-ethyl)-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid(1025902-00-4)

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: 1025902-00-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1025902-00-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,5,9,0 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1025902-00:
(9*1)+(8*0)+(7*2)+(6*5)+(5*9)+(4*0)+(3*2)+(2*0)+(1*0)=104
104 % 10 = 4
So 1025902-00-4 is a valid CAS Registry Number.

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1025902-00-4Relevant academic research and scientific papers

Asymmetric synthesis of quaternary tetrahydroisoquinoline-3-carboxylic acid derivatives

Alezra, Valérie,Bonin, Martine,Micouin, Laurent,Husson, Henri-Philippe

, p. 2111 - 2113 (2007/10/03)

A new route towards the asymmetric preparation of quaternary 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid derivatives has been developed. The key step involves an intramolecular Pictet-Spengler reaction of an oxazolidino ester.

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