Cas 74427-67-1,Acetic acid (2R,3R,4S,5R)-5-acetoxy-2-[bis-(2-chloro-ethyl)-amino]-3-hydroxy-tetrahydro-pyran-4-yl ester

74427-67-1

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Basic information

Product Name: Acetic acid (2R,3R,4S,5R)-5-acetoxy-2-[bis-(2-chloro-ethyl)-amino]-3-hydroxy-tetrahydro-pyran-4-yl ester
Synonyms: Acetic acid (2R,3R,4S,5R)-5-acetoxy-2-[bis-(2-chloro-ethyl)-amino]-3-hydroxy-tetrahydro-pyran-4-yl ester
CAS NO:74427-67-1
Molecular Formula:
Molecular Weight: 358.219
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)-5-acetoxy-2-[bis-(2-chloro-ethyl)-amino]-3-hydroxy-tetrahydro-pyran-4-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (2R,3R,4S,5R)-5-acetoxy-2-[bis-(2-chloro-ethyl)-amino]-3-hydroxy-tetrahydro-pyran-4-yl ester(74427-67-1)
EPA Substance Registry System: Acetic acid (2R,3R,4S,5R)-5-acetoxy-2-[bis-(2-chloro-ethyl)-amino]-3-hydroxy-tetrahydro-pyran-4-yl ester(74427-67-1)

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: 74427-67-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 74427-67-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,4,2 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 74427-67:
(7*7)+(6*4)+(5*4)+(4*2)+(3*7)+(2*6)+(1*7)=141
141 % 10 = 1
So 74427-67-1 is a valid CAS Registry Number.

74427-67-1Upstream product

74427-67-1Downstream Products

74427-66-0 tri-O-acetyl-2,3,4 -1-desoxy-1 β-D-rybopyrannose

74427-67-1Relevant academic research and scientific papers

Synthesis and biological activity of nitrogen mustards carbohydrate derivatives

Moruzzi,Montero,Imbach

, p. 125 - 132 (2007/10/02)

The authors describe the synthesis of N,N-bis(2-chloroethyl) amine carbohydrate derivatives, using sugar moieties previously associated with other oncostatic agents. The structure of these compounds was determined using 1H and 13C NMR spectroscopy. Their antitumor activity on L1210 on mice and their immunodepressive effects have been evaluated.

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