Cas 1050264-70-4,(1S,2R,4R)-N-(2-carboxy-4,5-dichlorobenzoyl)-10,2-camphorsultam ester of (3S)-(+)-3-benzyl-4-(N,N-diisopropylureido)-1,3-butandiol

1050264-70-4

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Basic information

Product Name: (1S,2R,4R)-N-(2-carboxy-4,5-dichlorobenzoyl)-10,2-camphorsultam ester of (3S)-(+)-3-benzyl-4-(N,N-diisopropylureido)-1,3-butandiol
Synonyms: (1S,2R,4R)-N-(2-carboxy-4,5-dichlorobenzoyl)-10,2-camphorsultam ester of (3S)-(+)-3-benzyl-4-(N,N-diisopropylureido)-1,3-butandiol
CAS NO:1050264-70-4
Molecular Formula:
Molecular Weight: 736.757
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,2R,4R)-N-(2-carboxy-4,5-dichlorobenzoyl)-10,2-camphorsultam ester of (3S)-(+)-3-benzyl-4-(N,N-diisopropylureido)-1,3-butandiol(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2R,4R)-N-(2-carboxy-4,5-dichlorobenzoyl)-10,2-camphorsultam ester of (3S)-(+)-3-benzyl-4-(N,N-diisopropylureido)-1,3-butandiol(1050264-70-4)
EPA Substance Registry System: (1S,2R,4R)-N-(2-carboxy-4,5-dichlorobenzoyl)-10,2-camphorsultam ester of (3S)-(+)-3-benzyl-4-(N,N-diisopropylureido)-1,3-butandiol(1050264-70-4)

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: 1050264-70-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1050264-70-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,0,2,6 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1050264-70:
(9*1)+(8*0)+(7*5)+(6*0)+(5*2)+(4*6)+(3*4)+(2*7)+(1*0)=104
104 % 10 = 4
So 1050264-70-4 is a valid CAS Registry Number.

1050264-70-4Upstream product

1050264-70-4Downstream Products

1050264-76-0 (3S)-(-)-3-benzyl-4-(N,N-diisopropylureido)-1,3-butandiol

1050264-70-4Relevant academic research and scientific papers

Chirality transfer from epoxide to carbanion: Base-induced alkylation of O-carbamoyl cyanohydrins of β-silyl-α,β-epoxy aldehyde

Sasaki, Michiko,Kawanishi, Eiji,Shirakawa, Yuri,Kawahata, Masatoshi,Masu, Hyuma,Yamaguchi, Kentaro,Takeda, Kei

supporting information; experimental part, p. 3061 - 3064 (2009/05/26)

Enantioselective C-C bond formation at an α-position of a nitrile group with an external electrophile can be realized, although in modest ee, with the aid of both the concerted process of an epoxysilane rearrangement and a carbamoyl group. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

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