Cas 131682-24-1,(1R,2R,3R,4S)-1-(Z-2'-cyano-2'-tert-butylmercaptoethenylamino)-2,3-diacetoxy-4-hydroxycyclohex-5-ene

131682-24-1

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Basic information

Product Name: (1R,2R,3R,4S)-1-(Z-2'-cyano-2'-tert-butylmercaptoethenylamino)-2,3-diacetoxy-4-hydroxycyclohex-5-ene
Synonyms:
CAS NO:131682-24-1
Molecular Formula:
Molecular Weight: 368.454
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: (1R,2R,3R,4S)-1-(Z-2'-cyano-2'-tert-butylmercaptoethenylamino)-2,3-diacetoxy-4-hydroxycyclohex-5-ene(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2R,3R,4S)-1-(Z-2'-cyano-2'-tert-butylmercaptoethenylamino)-2,3-diacetoxy-4-hydroxycyclohex-5-ene(131682-24-1)
EPA Substance Registry System: (1R,2R,3R,4S)-1-(Z-2'-cyano-2'-tert-butylmercaptoethenylamino)-2,3-diacetoxy-4-hydroxycyclohex-5-ene(131682-24-1)

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: 131682-24-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 131682-24-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,6,8 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 131682-24:
(8*1)+(7*3)+(6*1)+(5*6)+(4*8)+(3*2)+(2*2)+(1*4)=111
111 % 10 = 1
So 131682-24-1 is a valid CAS Registry Number.

131682-24-1Upstream product

131603-42-4 (1S,4R,7S,8R)-7,8-diacetoxy-3-(2'-cyano-2'-tert-butylmercaptoethenyl)-3-aza-2-oxabicyclo<2.2.2>oct-5-ene

131682-24-1Downstream Products

131682-24-1Relevant academic research and scientific papers

SYNTHESIS OF CHIRAL AMINOCYCLITOLS VIA EPOXYEPIMINATION

Braun, H.,Burger, W.,Kresze, G.,Schmidtchen, F. P.,Vaerman, J. L.,Viehe, H. G.

, p. 403 - 415 (1990)

Asymmetric Hetero-Diels-Alder reactions of cyclohexadienes 1 and (+/-)2 with the α-chloronitroso derivative of D-mannose 6 give the chiral dihydrooxazines 3-5.After N-functionalisation with the chloro-olefin 10 the N-vinyl-dihydrooxazines 11-13 thermally

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