Cas 913183-46-7,(1'S,4R,6S,8S)-9-(tert-butyldiphenylsilyloxy)-4,6,8-trimethyl-N-(1'-phenylethyl)nonaneamide

913183-46-7

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Basic information

Product Name: (1'S,4R,6S,8S)-9-(tert-butyldiphenylsilyloxy)-4,6,8-trimethyl-N-(1'-phenylethyl)nonaneamide
Synonyms: (1'S,4R,6S,8S)-9-(tert-butyldiphenylsilyloxy)-4,6,8-trimethyl-N-(1'-phenylethyl)nonaneamide
CAS NO:913183-46-7
Molecular Formula:
Molecular Weight: 557.892
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: (1'S,4R,6S,8S)-9-(tert-butyldiphenylsilyloxy)-4,6,8-trimethyl-N-(1'-phenylethyl)nonaneamide(CAS DataBase Reference)
NIST Chemistry Reference: (1'S,4R,6S,8S)-9-(tert-butyldiphenylsilyloxy)-4,6,8-trimethyl-N-(1'-phenylethyl)nonaneamide(913183-46-7)
EPA Substance Registry System: (1'S,4R,6S,8S)-9-(tert-butyldiphenylsilyloxy)-4,6,8-trimethyl-N-(1'-phenylethyl)nonaneamide(913183-46-7)

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: 913183-46-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 913183-46-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,3,1,8 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 913183-46:
(8*9)+(7*1)+(6*3)+(5*1)+(4*8)+(3*3)+(2*4)+(1*6)=157
157 % 10 = 7
So 913183-46-7 is a valid CAS Registry Number.

913183-46-7Upstream product

913183-45-6 (2E,1'S,4S,6S,8S)-9-(tert-butyldiphenylsilyloxy)-4,6,8-trimethyl-N-(1'-phenylethyl)non-2-eneamide

913183-46-7Downstream Products

913183-46-7Relevant academic research and scientific papers

Synthesis of the C1-C16 fragment of ionomycin using a neutral (η3-allyl)iron complex

Cooksey, John P.,Kocienski, Philip J.,Li, Ying-Fa,Schunk, Stefan,Snaddon, Thomas N.

, p. 3325 - 3336 (2008/09/16)

Key steps in the synthesis of the C1-C16 polyketide fragment of ionomycin were the nucleophilic addition of an organocuprate to a neutral (η3-allyl)iron complex and the construction of a β-diketone moiety by the Rh-catalysed rearrangement of an

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