Cas 3371-38-8,1L-2-O-Methyl-1-O-p-tolylsulfonyl-chiro-inosit

3371-38-8

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Basic information

Product Name: 1L-2-O-Methyl-1-O-p-tolylsulfonyl-chiro-inosit
Synonyms:
CAS NO:3371-38-8
Molecular Formula:
Molecular Weight: 348.374
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: 1L-2-O-Methyl-1-O-p-tolylsulfonyl-chiro-inosit(CAS DataBase Reference)
NIST Chemistry Reference: 1L-2-O-Methyl-1-O-p-tolylsulfonyl-chiro-inosit(3371-38-8)
EPA Substance Registry System: 1L-2-O-Methyl-1-O-p-tolylsulfonyl-chiro-inosit(3371-38-8)

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: 3371-38-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 3371-38-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,7 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3371-38:
(6*3)+(5*3)+(4*7)+(3*1)+(2*3)+(1*8)=78
78 % 10 = 8
So 3371-38-8 is a valid CAS Registry Number.

3371-38-8Upstream product

3371-38-8Downstream Products

18391-41-8 (-)-1-O-Methyl-allo-inosit-pentaacetat

3371-38-8Relevant academic research and scientific papers

Cyclitol Reactions, V. - Synthesis of Enantiomerically Pure Valienamine from Quebrachitol

Paulsen, Hans,Heiker, Fred R.

, p. 2180 - 2203 (2007/10/02)

An enantioselective synthesis of Valienamine (86) from quebrachitol (L-2O-methyl-chiro-inositol) (1) is described.Valienamine (86) is an unsaturated branched-chain aminocyclitol found in the central structural unit of the antidiabetic drug acarbose.Techniques for the introduction of side chains, azido groups, and double bonds into inositol systems are investigated.The methods developed in this connection are applied in the synthesis of valienamine.

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