Cas 1242079-38-4,methyl (3,5-bis[4-(1R,2S)-(2-hydroxy-1-methyl-2-phenylethyliminomethyl)benzyloxy])benzoate

1242079-38-4

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Basic information

Product Name: methyl (3,5-bis[4-(1R,2S)-(2-hydroxy-1-methyl-2-phenylethyliminomethyl)benzyloxy])benzoate
Synonyms: methyl (3,5-bis[4-(1R,2S)-(2-hydroxy-1-methyl-2-phenylethyliminomethyl)benzyloxy])benzoate
CAS NO:1242079-38-4
Molecular Formula:
Molecular Weight: 670.805
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: methyl (3,5-bis[4-(1R,2S)-(2-hydroxy-1-methyl-2-phenylethyliminomethyl)benzyloxy])benzoate(CAS DataBase Reference)
NIST Chemistry Reference: methyl (3,5-bis[4-(1R,2S)-(2-hydroxy-1-methyl-2-phenylethyliminomethyl)benzyloxy])benzoate(1242079-38-4)
EPA Substance Registry System: methyl (3,5-bis[4-(1R,2S)-(2-hydroxy-1-methyl-2-phenylethyliminomethyl)benzyloxy])benzoate(1242079-38-4)

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: 1242079-38-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1242079-38-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,2,0,7 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1242079-38:
(9*1)+(8*2)+(7*4)+(6*2)+(5*0)+(4*7)+(3*9)+(2*3)+(1*8)=134
134 % 10 = 4
So 1242079-38-4 is a valid CAS Registry Number.

1242079-38-4Upstream product

37577-28-9 (1S,2R)-(+)-norphedrine

1242079-38-4Downstream Products

1242079-38-4Relevant academic research and scientific papers

Chiral modification of polyformyl compounds of dendrite type with optically active primary and secondary 1,2-aminoalcohols

Kelbysheva,Pleshkova,Lyubimov,Dolgova,Loim

, p. 260 - 267 (2010)

Procedures were developed for preparation of optically active dendrones and dendrimers with terminal 1,2-hydroxylimino, 1,2-hydroxylamino and oxazolidinyl groups containing ether bonds in the branches and ester bonds in the backbone of the macromolecule.

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