Cas 1360545-82-9,methyl (3R,4R,5R,6R)-6-(2,2-diethoxyethyl)-3-ethyl-2-hydroxy-4-(4-methoxy-4-oxobutyl)-5-nitrocyclohex-1-enecarboxylate

1360545-82-9

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Basic information

Product Name: methyl (3R,4R,5R,6R)-6-(2,2-diethoxyethyl)-3-ethyl-2-hydroxy-4-(4-methoxy-4-oxobutyl)-5-nitrocyclohex-1-enecarboxylate
Synonyms:
CAS NO:1360545-82-9
Molecular Formula:
Molecular Weight: 445.51
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: methyl (3R,4R,5R,6R)-6-(2,2-diethoxyethyl)-3-ethyl-2-hydroxy-4-(4-methoxy-4-oxobutyl)-5-nitrocyclohex-1-enecarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl (3R,4R,5R,6R)-6-(2,2-diethoxyethyl)-3-ethyl-2-hydroxy-4-(4-methoxy-4-oxobutyl)-5-nitrocyclohex-1-enecarboxylate(1360545-82-9)
EPA Substance Registry System: methyl (3R,4R,5R,6R)-6-(2,2-diethoxyethyl)-3-ethyl-2-hydroxy-4-(4-methoxy-4-oxobutyl)-5-nitrocyclohex-1-enecarboxylate(1360545-82-9)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1360545-82-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1360545-82-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,0,5,4 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1360545-82:
(9*1)+(8*3)+(7*6)+(6*0)+(5*5)+(4*4)+(3*5)+(2*8)+(1*2)=149
149 % 10 = 9
So 1360545-82-9 is a valid CAS Registry Number.

1360545-82-9Upstream product

1360545-82-9Downstream Products

16625-37-9 stenine

1360545-82-9Relevant academic research and scientific papers

Enantioselective total synthesis of (-)- Stenine

Chen, Jingbo,Chen, Jingchao,Xie, Yan,Zhang, Hongbin

, p. 1024 - 1027 (2012)

In control: (-)-Stenine has been synthesized in 14 steps from commercially available compounds with an overall yield of 5.9 % by using a method that is based on double Michael addition. In the key step, the stereogenic centers that are required for (-)-stenine are generated in a highly stereocontrolled, asymmetric, one-pot cyclization to give a densely substituted cyclohexane core. Copyright

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