Cas 1450754-63-8,(1S)-2-hydroxy-1-[(1S,6R)-3-methyl-6-cyanocyclohex-3-en-1-yl]ethyl formate

1450754-63-8

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Basic information

Product Name: (1S)-2-hydroxy-1-[(1S,6R)-3-methyl-6-cyanocyclohex-3-en-1-yl]ethyl formate
Synonyms: (1S)-2-hydroxy-1-[(1S,6R)-3-methyl-6-cyanocyclohex-3-en-1-yl]ethyl formate
CAS NO:1450754-63-8
Molecular Formula:
Molecular Weight: 209.245
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: (1S)-2-hydroxy-1-[(1S,6R)-3-methyl-6-cyanocyclohex-3-en-1-yl]ethyl formate(CAS DataBase Reference)
NIST Chemistry Reference: (1S)-2-hydroxy-1-[(1S,6R)-3-methyl-6-cyanocyclohex-3-en-1-yl]ethyl formate(1450754-63-8)
EPA Substance Registry System: (1S)-2-hydroxy-1-[(1S,6R)-3-methyl-6-cyanocyclohex-3-en-1-yl]ethyl formate(1450754-63-8)

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: 1450754-63-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1450754-63-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,0,7,5 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1450754-63:
(9*1)+(8*4)+(7*5)+(6*0)+(5*7)+(4*5)+(3*4)+(2*6)+(1*3)=158
158 % 10 = 8
So 1450754-63-8 is a valid CAS Registry Number.

1450754-63-8Upstream product

1450753-19-1 (1S,2S,7R,9R)-4-methyl-10,12-dioxatricyclo[7.2.1.0^2,7]dodec-4-en-8-one syn-oxime

1450754-63-8Downstream Products

1450754-63-8Relevant academic research and scientific papers

Eleuthesides and their analogs: III. Reaction of Red-Al with γ,δ-epoxy nitriles

Khalilova, Yu. A.,Doronina, O. Yu.,Sharipov,Spirikhin,Valeev

, p. 986 - 994 (2013/09/02)

Oxiranyl-substituted cycloalkenecarbonitriles obtained by the Beckmann fragmentation of oximes derived from levoglucosenone adducts with 1,3-butadiene, isoprene, cyclohexadiene, and cyclopentadiene were subjected to Red-Al reduction with opening of the ep

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