Cas 1235984-08-3,3-amino-2,6-anhydro-1,4-di-O-benzyl-5-carbamoyl-3,5-dideoxy-D-arabino-hex-5-enitol

1235984-08-3

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Basic information

Product Name: 3-amino-2,6-anhydro-1,4-di-O-benzyl-5-carbamoyl-3,5-dideoxy-D-arabino-hex-5-enitol
Synonyms: 3-amino-2,6-anhydro-1,4-di-O-benzyl-5-carbamoyl-3,5-dideoxy-D-arabino-hex-5-enitol
CAS NO:1235984-08-3
Molecular Formula:
Molecular Weight: 368.433
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: 3-amino-2,6-anhydro-1,4-di-O-benzyl-5-carbamoyl-3,5-dideoxy-D-arabino-hex-5-enitol(CAS DataBase Reference)
NIST Chemistry Reference: 3-amino-2,6-anhydro-1,4-di-O-benzyl-5-carbamoyl-3,5-dideoxy-D-arabino-hex-5-enitol(1235984-08-3)
EPA Substance Registry System: 3-amino-2,6-anhydro-1,4-di-O-benzyl-5-carbamoyl-3,5-dideoxy-D-arabino-hex-5-enitol(1235984-08-3)

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: 1235984-08-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1235984-08-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,5,9,8 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1235984-08:
(9*1)+(8*2)+(7*3)+(6*5)+(5*9)+(4*8)+(3*4)+(2*0)+(1*8)=173
173 % 10 = 3
So 1235984-08-3 is a valid CAS Registry Number.

1235984-08-3Upstream product

1235984-04-9 2,6-anhydro-3-azido-1,4-di-O-benzyl-5-carbamoyl-3,5-dideoxy-D-arabino-hex-5-enitol

1235984-08-3Downstream Products

1235984-08-3Relevant academic research and scientific papers

Synthesis of γ-aminobutyric acid analogs based on carbohydrate scaffolds

Zhong, Ming,Meng, Xiang-Bao,Li, Zhong-Jun

experimental part, p. 1099 - 1106 (2010/09/12)

γ-Aminobutyric acid analogs based on sugar scaffolds were prepared in six to nine steps starting from d-glucal and d-galactal. The key step in the synthesis is the Vilsmeier-Haack reaction that affords the corresponding 2-C-formyl glycal on treatment with

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