Cas 40437-20-5,O4,O6-(Ξ)-benzylidene-2-benzyloxycarbonylamino-D-2-deoxy-gluconic acid

40437-20-5

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Basic information

Product Name: O⁴,O⁶-(Ξ)-benzylidene-2-benzyloxycarbonylamino-D-2-deoxy-gluconic acid
Synonyms: O⁴,O⁶-(Ξ)-benzylidene-2-benzyloxycarbonylamino-D-2-deoxy-gluconic acid
CAS NO:40437-20-5
Molecular Formula:
Molecular Weight: 417.416
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: O⁴,O⁶-(Ξ)-benzylidene-2-benzyloxycarbonylamino-D-2-deoxy-gluconic acid(CAS DataBase Reference)
NIST Chemistry Reference: O⁴,O⁶-(Ξ)-benzylidene-2-benzyloxycarbonylamino-D-2-deoxy-gluconic acid(40437-20-5)
EPA Substance Registry System: O⁴,O⁶-(Ξ)-benzylidene-2-benzyloxycarbonylamino-D-2-deoxy-gluconic acid(40437-20-5)

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: 40437-20-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 40437-20-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,4,3 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 40437-20:
(7*4)+(6*0)+(5*4)+(4*3)+(3*7)+(2*2)+(1*0)=85
85 % 10 = 5
So 40437-20-5 is a valid CAS Registry Number.

40437-20-5Upstream product

40149-86-8 ethyl 4,6-O-benzylidene-2-<(N-Z)-amino>-2-deoxy-D-gluconate

40437-20-5Downstream Products

65025-39-0 2-benzyloxycarbonylamino-4,6-O-benzylidene-2,3-dideoxy-D-erythro-hex-2-eno-1,5-lactone

40437-20-5Relevant academic research and scientific papers

SYNTHESIS OF PEPTIDES CONTAINING D-GLUCOSAMINIC ACID, I. SYNTHETIC METHODS

Deak, Gy.,Gall-Istok, K.,Zara-Kaczian, E.,Kisfaludy, L.

, p. 375 - 384 (2007/10/02)

The azide method has been found suitable for the preparation of peptides containing D-glucosaminic acid as the N-terminal amino acid, protected from lactonization in the form of the 4,6-O-benzylidene derivative.When acted upon by dicyclohexylcarbodiimide,

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