Cas 1007389-77-6,N-(phenylmethoxy)-N-2-propyn-1-ylcarbamic acid 1,1-dimethylethyl ester

1007389-77-6

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Basic information

Product Name: N-(phenylmethoxy)-N-2-propyn-1-ylcarbamic acid 1,1-dimethylethyl ester
Synonyms: N-(phenylmethoxy)-N-2-propyn-1-ylcarbamic acid 1,1-dimethylethyl ester
CAS NO:1007389-77-6
Molecular Formula:
Molecular Weight: 261.321
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: N-(phenylmethoxy)-N-2-propyn-1-ylcarbamic acid 1,1-dimethylethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: N-(phenylmethoxy)-N-2-propyn-1-ylcarbamic acid 1,1-dimethylethyl ester(1007389-77-6)
EPA Substance Registry System: N-(phenylmethoxy)-N-2-propyn-1-ylcarbamic acid 1,1-dimethylethyl ester(1007389-77-6)

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: 1007389-77-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1007389-77-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,7,3,8 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1007389-77:
(9*1)+(8*0)+(7*0)+(6*7)+(5*3)+(4*8)+(3*9)+(2*7)+(1*7)=146
146 % 10 = 6
So 1007389-77-6 is a valid CAS Registry Number.

1007389-77-6Upstream product

1007389-77-6Downstream Products

1007389-77-6Relevant academic research and scientific papers

Cascade radical reaction of substrates with a carbon-carbon triple bond as a radical acceptor

Miyabe, Hideto,Asada, Ryuta,Takemoto, Yoshiji

supporting information, p. 1148 - 1155 (2013/07/26)

The limitation of hydroxamate ester as a chiral Lewis acid coordination moiety was first shown in an intermolecular reaction involving a radical addition and sequential allylation processes. Next, the effect of hydroxamate ester was studied in the cascade

Polarity-mismatched addition of electrophilic carbon radicals to an electron-deficient acceptor: Cascade radical addition-cyclization-trapping reaction

Yoshioka, Eito,Kohtani, Shigeru,Sawai, Kaori,Kentefu,Tanaka, Eri,Miyabe, Hideto

, p. 8588 - 8604,17 (2020/09/15)

The polarity-mismatched perfluoroalkyl radical addition to electron-deficient alkenes was studied. For this study, several substrates having two polarity-different radical acceptors were employed to investigate the regiochemical courses of cascade reactio

A dramatic effect of double bond configuration in N-oxy-3-aza Cope rearrangements-a simple synthesis of functionalised allenes

Pinto, Luis F.V.,Glória, Paulo M.C.,Gomes, Mário J.S.,Rzepa, Henry S.,Prabhakar, Sundaresan,Lobo, Ana M.

experimental part, p. 3446 - 3449 (2009/09/25)

The first examples of low temperature N-oxy-3-aza Cope rearrangements, leading to functionalised allenes are described, where the Z-configuration of the enaminic double bond in the rearranging system proves critical.

Enantioselective cascade radical addition-cyclization-trapping reactions

Miyabe, Hideto,Asada, Ryuta,Toyoda, Akira,Takemoto, Yoshiji

, p. 5863 - 5866 (2007/10/03)

(Chemical Equation Presented) In addition: The chiral Lewis acid mediated radical addition-cyclization-trapping reaction of a hydroxamate ester with two radical acceptors provides a cascade approach for the asymmetric synthesis of various γ-lactams (see s

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