Cas 162414-07-5,N-<(1S)-(1,2,4/3,5)-2,3,4-trihydroxy-5-(hydroxymethyl)cyclohexyl>-N'-(2',3',4',6'-tetra-O-benzyl-α-D-glucopyranosyl)thiourea

162414-07-5

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Basic information

Product Name: N-<(1S)-(1,2,4/3,5)-2,3,4-trihydroxy-5-(hydroxymethyl)cyclohexyl>-N'-(2',3',4',6'-tetra-O-benzyl-α-D-glucopyranosyl)thiourea
Synonyms: N-<(1S)-(1,2,4/3,5)-2,3,4-trihydroxy-5-(hydroxymethyl)cyclohexyl>-N'-(2',3',4',6'-tetra-O-benzyl-α-D-glucopyranosyl)thiourea
CAS NO:162414-07-5
Molecular Formula:
Molecular Weight: 758.933
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: N-<(1S)-(1,2,4/3,5)-2,3,4-trihydroxy-5-(hydroxymethyl)cyclohexyl>-N'-(2',3',4',6'-tetra-O-benzyl-α-D-glucopyranosyl)thiourea(CAS DataBase Reference)
NIST Chemistry Reference: N-<(1S)-(1,2,4/3,5)-2,3,4-trihydroxy-5-(hydroxymethyl)cyclohexyl>-N'-(2',3',4',6'-tetra-O-benzyl-α-D-glucopyranosyl)thiourea(162414-07-5)
EPA Substance Registry System: N-<(1S)-(1,2,4/3,5)-2,3,4-trihydroxy-5-(hydroxymethyl)cyclohexyl>-N'-(2',3',4',6'-tetra-O-benzyl-α-D-glucopyranosyl)thiourea(162414-07-5)

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: 162414-07-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 162414-07-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,4,1 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 162414-07:
(8*1)+(7*6)+(6*2)+(5*4)+(4*1)+(3*4)+(2*0)+(1*7)=105
105 % 10 = 5
So 162414-07-5 is a valid CAS Registry Number.

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162414-07-5Relevant academic research and scientific papers

Synthesis of Trehazolin Analogues containing Modified Aminocyclitol Moieties

Uchida, Chikara,Kitahashi, Hideo,Yamagishi, Tatsuya,Iwaisaki, Yoko,Ogawa, Seiichiro

, p. 2775 - 2786 (2007/10/02)

In order to elucidate structure-activity relationships of the trehalase inhibitor trehazolin 1, three analogues: deoxytrehazolin D-2, and de(hydroxymethyl)trehazolin D-3 and its diastereomer L-3 were synthesized by coupling of the sugar isothiocyanate 18

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