Cas 13407-28-8,3-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-16-dehydropregnanolone

13407-28-8

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Basic information

Product Name: 3-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-16-dehydropregnanolone
Synonyms: 3-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-16-dehydropregnanolone
CAS NO:13407-28-8
Molecular Formula:
Molecular Weight: 644.76
EINECS: N/A
Product Categories: N/A
Mol File: 13407-28-8.mol
Article Data: 1

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: 3-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-16-dehydropregnanolone(CAS DataBase Reference)
NIST Chemistry Reference: 3-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-16-dehydropregnanolone(13407-28-8)
EPA Substance Registry System: 3-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-16-dehydropregnanolone(13407-28-8)

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: 13407-28-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 13407-28-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,0 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13407-28:
(7*1)+(6*3)+(5*4)+(4*0)+(3*7)+(2*2)+(1*8)=78
78 % 10 = 8
So 13407-28-8 is a valid CAS Registry Number.

13407-28-8Upstream product

58026-06-5 3',4',6'-tri-O-acetyl-1',2',O-(16-dehydropregnenolone-3-yloxyethylidene)-α-D-glucopyranose

13407-28-8Downstream Products

13407-28-8Relevant articles and documents

CATALYTIC REARRANGEMENT OF α-D-GLUCOSE 1,2-ORTHOACETATE DERIVATIVES OF PREGNENOLONE AND 16-DEHYDROPREGNENOLONE

Samoshina, N. F.,Denisenko, V. A.,Novikov, V. L.,Uvarova, N. I.

, p. 177 - 182 (2007/10/02)

The rearrangement of pregnenolone and 16-dehydropregnenolone α-D-glucose orthoacetates in the presence of mercuric bromide is, because of the high specific selectivity and satisfactory yields of the desired β-D-glucosides, the most effective method of glycosylating the steroids mentioned.

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