Cas 72045-41-1,Acetic acid (2R,3R,4S,5R,6S)-4,5,6-tris-benzyloxy-3-hydroxy-tetrahydro-pyran-2-ylmethyl ester

72045-41-1

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Basic information

Product Name: Acetic acid (2R,3R,4S,5R,6S)-4,5,6-tris-benzyloxy-3-hydroxy-tetrahydro-pyran-2-ylmethyl ester
Synonyms: Acetic acid (2R,3R,4S,5R,6S)-4,5,6-tris-benzyloxy-3-hydroxy-tetrahydro-pyran-2-ylmethyl ester
CAS NO:72045-41-1
Molecular Formula:
Molecular Weight: 492.569
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: Acetic acid (2R,3R,4S,5R,6S)-4,5,6-tris-benzyloxy-3-hydroxy-tetrahydro-pyran-2-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (2R,3R,4S,5R,6S)-4,5,6-tris-benzyloxy-3-hydroxy-tetrahydro-pyran-2-ylmethyl ester(72045-41-1)
EPA Substance Registry System: Acetic acid (2R,3R,4S,5R,6S)-4,5,6-tris-benzyloxy-3-hydroxy-tetrahydro-pyran-2-ylmethyl ester(72045-41-1)

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: 72045-41-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 72045-41-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,0,4 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 72045-41:
(7*7)+(6*2)+(5*0)+(4*4)+(3*5)+(2*4)+(1*1)=101
101 % 10 = 1
So 72045-41-1 is a valid CAS Registry Number.

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72045-41-1Relevant academic research and scientific papers

HYDRAZINEDITHIOCARBONATE (HDTC) AS A NEW REAGENT FOR THE IMPROVED REMOVAL OF CHLOROACETYL AND BROMOACETYL PROTECTIVE GROUPS.

Boeckel, C.A.A. van,Beetz, T.

, p. 3775 - 3778 (1983)

The use of hydrazinedithiocarbonate (HDTC) for the removal of chloroacetyl and bromoacetyl groups is described.The advantage of this reagent is the selective deprotection under mild conditions, which was demonstrated on carbohydrate derivatives.

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