Cas 1312425-25-4,benzyl 2,3-O-isopropylidene-4-O-acetyl-6-O-tert-butyldiphenylsilyl-α-D-mannopyranoside

1312425-25-4

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Basic information

Product Name: benzyl 2,3-O-isopropylidene-4-O-acetyl-6-O-tert-butyldiphenylsilyl-α-D-mannopyranoside
Synonyms: benzyl 2,3-O-isopropylidene-4-O-acetyl-6-O-tert-butyldiphenylsilyl-α-D-mannopyranoside
CAS NO:1312425-25-4
Molecular Formula:
Molecular Weight: 590.789
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: benzyl 2,3-O-isopropylidene-4-O-acetyl-6-O-tert-butyldiphenylsilyl-α-D-mannopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: benzyl 2,3-O-isopropylidene-4-O-acetyl-6-O-tert-butyldiphenylsilyl-α-D-mannopyranoside(1312425-25-4)
EPA Substance Registry System: benzyl 2,3-O-isopropylidene-4-O-acetyl-6-O-tert-butyldiphenylsilyl-α-D-mannopyranoside(1312425-25-4)

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: 1312425-25-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1312425-25-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,2,4,2 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1312425-25:
(9*1)+(8*3)+(7*1)+(6*2)+(5*4)+(4*2)+(3*5)+(2*2)+(1*5)=104
104 % 10 = 4
So 1312425-25-4 is a valid CAS Registry Number.

1312425-25-4Upstream product

1312425-25-4Downstream Products

1312425-26-5 benzyl 4-O-acetyl-6-O-tert-butyldiphenylsilyl-α-D-mannopyranoside

1312425-25-4Relevant academic research and scientific papers

Four-component one-pot synthesis of a branched manno-pentasaccharide: Tert-butyldiphenylsilyl ether as an in situ removable carbohydrate-protecting group

Sarkar, Swarbhanu,Dutta, Samrat,Das, Gora,Sen, Asish Kumar

, p. 4118 - 4122 (2011)

A branched mannose-pentasaccharide was synthesized in a convergent one-pot sequence involving chemo- and regioselective glycosylations of suitable acceptors and in situ removal of tert-butyldiphenylsilyl group. The process demonstrated that a combination

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